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Artigo de periodico
Hemiarhinia caused by a missense variation in SMCHD1: a mild phenotype in the clinical spectrum of Bosma arhinia microphthalmia syndrome (2024)
Kokitsu-Nakata, Nancy Mizue ; Segarra, Vinicius Contrucci Dantas ; Tonello, Cristiano ; Brandão, Michele Madeira ; Alonso, Nivaldo ; Zechi-Ceide, Roseli Maria
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, FOB, HRACF
Subjects: HIPOGONADISMO, ANORMALIDADES CRANIOFACIAIS
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ABNT
KOKITSU-NAKATA, Nancy Mizue et al. Hemiarhinia caused by a missense variation in SMCHD1: a mild phenotype in the clinical spectrum of Bosma arhinia microphthalmia syndrome. American Journal of Medical Genetics. Part A, v. 194, n. 10, 2024Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63640. Acesso em: 17 nov. 2024.
APA
Kokitsu-Nakata, N. M., Segarra, V. C. D., Tonello, C., Brandão, M. M., Alonso, N., & Zechi-Ceide, R. M. (2024). Hemiarhinia caused by a missense variation in SMCHD1: a mild phenotype in the clinical spectrum of Bosma arhinia microphthalmia syndrome. American Journal of Medical Genetics. Part A, 194( 10). doi:10.1002/ajmg.a.63640
NLM
Kokitsu-Nakata NM, Segarra VCD, Tonello C, Brandão MM, Alonso N, Zechi-Ceide RM. Hemiarhinia caused by a missense variation in SMCHD1: a mild phenotype in the clinical spectrum of Bosma arhinia microphthalmia syndrome [Internet]. American Journal of Medical Genetics. Part A. 2024 ; 194( 10):[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.63640
Vancouver
Kokitsu-Nakata NM, Segarra VCD, Tonello C, Brandão MM, Alonso N, Zechi-Ceide RM. Hemiarhinia caused by a missense variation in SMCHD1: a mild phenotype in the clinical spectrum of Bosma arhinia microphthalmia syndrome [Internet]. American Journal of Medical Genetics. Part A. 2024 ; 194( 10):[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.63640
Artigo de periodico
Robin sequence facial profile after conservative treatment: a long-term follow-up (2024)
Siqueira, Gabriela Leticia Clavisio; Tonello, Cristiano ; Peixoto, Adriano Porto ; Daskalogiannakis, John ; Garib, Daniela Gamba ; Marques, Ilza Lazarini; Zechi-Ceide, Roseli Maria ; Alonso, Nivaldo ; Ozawa, Terumi Okada
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, FOB, FM, HRACF
Subjects: MICROGNATISMO, FOTOGRAFIA, SÍNDROME DE PIERRE ROBIN
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ABNT
SIQUEIRA, Gabriela Leticia Clavisio et al. Robin sequence facial profile after conservative treatment: a long-term follow-up. The Journal of Craniofacial Surgery, v. 35, n. Ja/Feb. 2024, p. 163-167, 2024Tradução . . Disponível em: http://dx.doi.org/10.1097/SCS.0000000000009749. Acesso em: 17 nov. 2024.
APA
Siqueira, G. L. C., Tonello, C., Peixoto, A. P., Daskalogiannakis, J., Garib, D. G., Marques, I. L., et al. (2024). Robin sequence facial profile after conservative treatment: a long-term follow-up. The Journal of Craniofacial Surgery, 35( Ja/Feb. 2024), 163-167. doi:10.1097/SCS.0000000000009749
NLM
Siqueira GLC, Tonello C, Peixoto AP, Daskalogiannakis J, Garib DG, Marques IL, Zechi-Ceide RM, Alonso N, Ozawa TO. Robin sequence facial profile after conservative treatment: a long-term follow-up [Internet]. The Journal of Craniofacial Surgery. 2024 ; 35( Ja/Feb. 2024): 163-167.[citado 2024 nov. 17 ] Available from: http://dx.doi.org/10.1097/SCS.0000000000009749
Vancouver
Siqueira GLC, Tonello C, Peixoto AP, Daskalogiannakis J, Garib DG, Marques IL, Zechi-Ceide RM, Alonso N, Ozawa TO. Robin sequence facial profile after conservative treatment: a long-term follow-up [Internet]. The Journal of Craniofacial Surgery. 2024 ; 35( Ja/Feb. 2024): 163-167.[citado 2024 nov. 17 ] Available from: http://dx.doi.org/10.1097/SCS.0000000000009749
Artigo de periodico
Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries (2024)
Mazzonetto, Patricia Camacho ; Villela, Darine ; Krepischi, Ana Cristina Victorino ; Pierry, Paulo Marques ; Bonaldi, Adriano; Almeida, Luiz Gustavo Dufner de ; Paula, Marcelo Gomes de ; Bürger, Matheus Carvalho ; Oliveira, Ana Gabriela de; Fonseca, Gustavo G. G; Giugliani, Roberto ; Riegel-Giugliani, Mariluce ; Bertola, Débora Romeo ; Yamamoto, Guilherme Lopes ; Passos-Bueno, Maria Rita ; Campos, Gabriele da Silva ; Machado, Ana Claudia Dantas ; Mazzeu, Juliana Forte ; Perrone, Eduardo ; Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy Mizue ; Vieira, Társis Paiva ; Steiner, Carlos Eduardo ; Gil-da-Silva-Lopes, Vera Lúcia ; Vieira, Daniela Koeller Rodrigues; Boy, Raquel ; Pina Neto, João Monteiro de ; Scapulatempo Neto, Cristovam ; Milanezi, Fernanda ; Rosenberg, Carla
Source: American Journal of Medical Genetics. Part A. Unidades: IB, BIOINFORMÁTICA, HRAC, FMRP
Subjects: CITOGENÉTICA, GENOMAS, CUIDADO PÓS-NATAL, DIAGNÓSTICO
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ABNT
MAZZONETTO, Patricia Camacho et al. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries. American Journal of Medical Genetics. Part A, v. No 2024, n. 11, p. e63802, 2024Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63802. Acesso em: 17 nov. 2024.
APA
Mazzonetto, P. C., Villela, D., Krepischi, A. C. V., Pierry, P. M., Bonaldi, A., Almeida, L. G. D. de, et al. (2024). Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries. American Journal of Medical Genetics. Part A, No 2024( 11), e63802. doi:10.1002/ajmg.a.63802
NLM
Mazzonetto PC, Villela D, Krepischi ACV, Pierry PM, Bonaldi A, Almeida LGD de, Paula MG de, Bürger MC, Oliveira AG de, Fonseca GGG, Giugliani R, Riegel-Giugliani M, Bertola DR, Yamamoto GL, Passos-Bueno MR, Campos G da S, Machado ACD, Mazzeu JF, Perrone E, Zechi-Ceide RM, Kokitsu-Nakata NM, Vieira TP, Steiner CE, Gil-da-Silva-Lopes VL, Vieira DKR, Boy R, Pina Neto JM de, Scapulatempo Neto C, Milanezi F, Rosenberg C. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries [Internet]. American Journal of Medical Genetics. Part A. 2024 ; No 2024( 11): e63802.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.63802
Vancouver
Mazzonetto PC, Villela D, Krepischi ACV, Pierry PM, Bonaldi A, Almeida LGD de, Paula MG de, Bürger MC, Oliveira AG de, Fonseca GGG, Giugliani R, Riegel-Giugliani M, Bertola DR, Yamamoto GL, Passos-Bueno MR, Campos G da S, Machado ACD, Mazzeu JF, Perrone E, Zechi-Ceide RM, Kokitsu-Nakata NM, Vieira TP, Steiner CE, Gil-da-Silva-Lopes VL, Vieira DKR, Boy R, Pina Neto JM de, Scapulatempo Neto C, Milanezi F, Rosenberg C. Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries [Internet]. American Journal of Medical Genetics. Part A. 2024 ; No 2024( 11): e63802.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.63802
Artigo de periodico
Systemic and oral abnormalities in Kabuki syndrome: a case series (2024)
Pinto, Lidiane de Castro ; Kokitsu-Nakata, Nancy Mizue ; Dalben, Gisele da Silva ; Azevedo-Silva, Lucas José de ; Almeida, Ana Lúcia Pompéia Fraga de
Source: Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. Unidades: HRAC, FOB, HRACF
Subjects: ANORMALIDADES CONGÊNITAS, DIAGNÓSTICO BUCAL, ABORDAGEM DE TRATAMENTO INTERDISCIPLINAR, FISSURA LÁBIOPALATINA
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ABNT
PINTO, Lidiane de Castro et al. Systemic and oral abnormalities in Kabuki syndrome: a case series. Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, v. 137, n. 5, p. e91-e98, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.oooo.2023.12.788. Acesso em: 17 nov. 2024.
APA
Pinto, L. de C., Kokitsu-Nakata, N. M., Dalben, G. da S., Azevedo-Silva, L. J. de, & Almeida, A. L. P. F. de. (2024). Systemic and oral abnormalities in Kabuki syndrome: a case series. Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 137( 5), e91-e98. doi:10.1016/j.oooo.2023.12.788
NLM
Pinto L de C, Kokitsu-Nakata NM, Dalben G da S, Azevedo-Silva LJ de, Almeida ALPF de. Systemic and oral abnormalities in Kabuki syndrome: a case series [Internet]. Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 2024 ; 137( 5): e91-e98.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.oooo.2023.12.788
Vancouver
Pinto L de C, Kokitsu-Nakata NM, Dalben G da S, Azevedo-Silva LJ de, Almeida ALPF de. Systemic and oral abnormalities in Kabuki syndrome: a case series [Internet]. Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 2024 ; 137( 5): e91-e98.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.oooo.2023.12.788
Artigo de periodico
Monodactyly in a patient with CHARGE syndrome: an additional case report (2024)
Serigatto, Henrique Regonaschi ; Zechi-Ceide, Roseli Maria ; Parizotto, Isabella ; Kokitsu-Nakata, Nancy Mizue
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, HRACF
Subjects: MONODACTYLIDAE, ANORMALIDADES CONGÊNITAS, FISSURA PALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERIGATTO, Henrique Regonaschi et al. Monodactyly in a patient with CHARGE syndrome: an additional case report. American Journal of Medical Genetics. Part A, v. 194, n. 6, 2024Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63561. Acesso em: 17 nov. 2024.
APA
Serigatto, H. R., Zechi-Ceide, R. M., Parizotto, I., & Kokitsu-Nakata, N. M. (2024). Monodactyly in a patient with CHARGE syndrome: an additional case report. American Journal of Medical Genetics. Part A, 194( 6). doi:10.1002/ajmg.a.63561
NLM
Serigatto HR, Zechi-Ceide RM, Parizotto I, Kokitsu-Nakata NM. Monodactyly in a patient with CHARGE syndrome: an additional case report [Internet]. American Journal of Medical Genetics. Part A. 2024 ; 194( 6):[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.63561
Vancouver
Serigatto HR, Zechi-Ceide RM, Parizotto I, Kokitsu-Nakata NM. Monodactyly in a patient with CHARGE syndrome: an additional case report [Internet]. American Journal of Medical Genetics. Part A. 2024 ; 194( 6):[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.63561
Artigo de periodico
Oculoauriculofrontonasal syndrome review: refining the phenotype through a new case series and literature (2023)
Serigatto, Henrique Regonaschi ; Kokitsu-Nakata, Nancy Mizue ; Vendramini-Pittoli, Siulan ; Tonello, Cristiano ; Moura, Priscila Padilha; Peixoto, Adriano Porto ; Gomes, Luiz Paulo; Zechi-Ceide, Roseli Maria
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, FOB, HRACF
Subjects: FISSURA PALATINA, ASSIMETRIA FACIAL, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERIGATTO, Henrique Regonaschi et al. Oculoauriculofrontonasal syndrome review: refining the phenotype through a new case series and literature. American Journal of Medical Genetics. Part A, v. No 2023, n. 11, p. 2493-2507, 2023Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63319. Acesso em: 17 nov. 2024.
APA
Serigatto, H. R., Kokitsu-Nakata, N. M., Vendramini-Pittoli, S., Tonello, C., Moura, P. P., Peixoto, A. P., et al. (2023). Oculoauriculofrontonasal syndrome review: refining the phenotype through a new case series and literature. American Journal of Medical Genetics. Part A, No 2023( 11), 2493-2507. doi:10.1002/ajmg.a.63319
NLM
Serigatto HR, Kokitsu-Nakata NM, Vendramini-Pittoli S, Tonello C, Moura PP, Peixoto AP, Gomes LP, Zechi-Ceide RM. Oculoauriculofrontonasal syndrome review: refining the phenotype through a new case series and literature [Internet]. American Journal of Medical Genetics. Part A. 2023 ; No 2023( 11): 2493-2507.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.63319
Vancouver
Serigatto HR, Kokitsu-Nakata NM, Vendramini-Pittoli S, Tonello C, Moura PP, Peixoto AP, Gomes LP, Zechi-Ceide RM. Oculoauriculofrontonasal syndrome review: refining the phenotype through a new case series and literature [Internet]. American Journal of Medical Genetics. Part A. 2023 ; No 2023( 11): 2493-2507.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.63319
Artigo de periodico
Craniocervical instability in oculoauriculovertebral spectrum (2023)
Gomes, Luiz Paulo; Ferraz, Beatriz Gonçalves ; Brandão, Michele Madeira ; Alonso, Nivaldo ; Pittoli, Siulan Vendramini ; Tonello, Cristiano
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, FOB, HRACF
Subjects: INSTABILIDADE ARTICULAR, COLUNA VERTEBRAL, SÍNDROME DE GOLDENHAR, ASSIMETRIA FACIAL
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ABNT
GOMES, Luiz Paulo et al. Craniocervical instability in oculoauriculovertebral spectrum. The Journal of Craniofacial Surgery, v. 34, n. 4, p. 1283-1286, 2023Tradução . . Disponível em: https://doi.org/10.1097/SCS.0000000000009192. Acesso em: 17 nov. 2024.
APA
Gomes, L. P., Ferraz, B. G., Brandão, M. M., Alonso, N., Pittoli, S. V., & Tonello, C. (2023). Craniocervical instability in oculoauriculovertebral spectrum. The Journal of Craniofacial Surgery, 34( 4), 1283-1286. doi:10.1097/SCS.0000000000009192
NLM
Gomes LP, Ferraz BG, Brandão MM, Alonso N, Pittoli SV, Tonello C. Craniocervical instability in oculoauriculovertebral spectrum [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 4): 1283-1286.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/SCS.0000000000009192
Vancouver
Gomes LP, Ferraz BG, Brandão MM, Alonso N, Pittoli SV, Tonello C. Craniocervical instability in oculoauriculovertebral spectrum [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 4): 1283-1286.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/SCS.0000000000009192
Artigo de periodico
Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies (2023)
Parizotto Paula, Isabella ; Gonçalves Paula, Raul ; Kokitsu-Nakata, Nancy Mizue ; Alonso, Nivaldo ; Tonello, Cristiano
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, FOB, HRACF
Subjects: OFTALMOPATIAS, ANORMALIDADES CONGÊNITAS, FISSURA LÁBIOPALATINA
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ABNT
PARIZOTTO PAULA, Isabella et al. Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies. The Journal of Craniofacial Surgery, v. 34, n. 6, p. e542-e546, 2023Tradução . . Disponível em: https://doi.org/10.1097/SCS.0000000000009557. Acesso em: 17 nov. 2024.
APA
Parizotto Paula, I., Gonçalves Paula, R., Kokitsu-Nakata, N. M., Alonso, N., & Tonello, C. (2023). Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies. The Journal of Craniofacial Surgery, 34( 6), e542-e546. doi:10.1097/SCS.0000000000009557
NLM
Parizotto Paula I, Gonçalves Paula R, Kokitsu-Nakata NM, Alonso N, Tonello C. Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 6): e542-e546.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/SCS.0000000000009557
Vancouver
Parizotto Paula I, Gonçalves Paula R, Kokitsu-Nakata NM, Alonso N, Tonello C. Clinical characterization of congenital anophthalmic and microphthalmic cavities in inidviduals with craniofacial anomalies [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 6): e542-e546.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/SCS.0000000000009557
Artigo de periodico
Craniofacial microsomia: new updates in spinal anomalies (2023)
Ferraz, Beatriz Gonçalves ; Vendramini-Pittoli, Siulan ; Gomes, Luiz Paulo; Brandão, Michele Madeira ; Alonso, Nivaldo ; Tonello, Cristiano
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, FOB, HRACF
Subjects: ASSIMETRIA FACIAL, SÍNDROME DE GOLDENHAR, COLUNA VERTEBRAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Beatriz Gonçalves et al. Craniofacial microsomia: new updates in spinal anomalies. The Journal of Craniofacial Surgery, v. 34, n. 4, p. e398-e401, 2023Tradução . . Disponível em: https://doi.org/10.1097/scs.0000000000009326. Acesso em: 17 nov. 2024.
APA
Ferraz, B. G., Vendramini-Pittoli, S., Gomes, L. P., Brandão, M. M., Alonso, N., & Tonello, C. (2023). Craniofacial microsomia: new updates in spinal anomalies. The Journal of Craniofacial Surgery, 34( 4), e398-e401. doi:10.1097/scs.0000000000009326
NLM
Ferraz BG, Vendramini-Pittoli S, Gomes LP, Brandão MM, Alonso N, Tonello C. Craniofacial microsomia: new updates in spinal anomalies [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 4): e398-e401.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/scs.0000000000009326
Vancouver
Ferraz BG, Vendramini-Pittoli S, Gomes LP, Brandão MM, Alonso N, Tonello C. Craniofacial microsomia: new updates in spinal anomalies [Internet]. The Journal of Craniofacial Surgery. 2023 ; 34( 4): e398-e401.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/scs.0000000000009326
Artigo de periodico
Phenotypic and mutational spectrum of ROR2-related Robinow syndrome (2022)
Lima, Ariadne R.; Ferreira, Barbara M.; Zhang, Chaofan; Jolly, Angad; Du, Haowei ; White, Janson J.; Dawood, Moez; Lins, Tulio C.; Chiabai, Marcela A.; van Beusekom, Ellen; Cordoba, Mara S.; Rosa, Erica C. C. Caldas; Kayserili, Hulya; Kimonis, Virginia; Wu, Erica; Mellado, Cecilia; Aggarwal, Vineet; Richieri-Costa, Antonio ; Brunoni, Décio; Canó, Talyta M.; Jorge, Alexander A. L. ; Kim, Chong Ae ; Honjo, Rachel ; Bertola, Débora R. ; Dandalo-Girardi, Raissa M.; Bayram, Yavuz; Gezdirici, Alper; Yilmaz-Gulec, Elif; Gumus, Evren; Yilmaz, Gülay C.; Okamoto, Nobuhiko ; Ohashi, Hirofumi; Coban–Akdemir, Zeynep; Mitani, Tadahiro; Jhangiani, Shalini N.; Muzny, Donna M.; Regattieri, Neysa A. P. ; Pogue, Robert ; Pereira, Rinaldo W.; Otto, Paulo A ; Gibbs, Richard A.; Ali, Bassam R.; van Bokhoven, Hans; Brunner, Han G.; Sutton, V. Reid; Lupski, James R. ; Vianna-Morgante, Angela M ; Carvalho, Claudia M. B. ; Mazzeu, Juliana F.
Source: Human Mutation. Unidades: HRAC, FM, IB
Subjects: FENÓTIPOS, MORFOLOGIA (ANATOMIA), SEQUENCIAMENTO GENÉTICO
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ABNT
LIMA, Ariadne R. et al. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human Mutation, v. 43, n. 7, p. 900-918, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24375. Acesso em: 17 nov. 2024.
APA
Lima, A. R., Ferreira, B. M., Zhang, C., Jolly, A., Du, H., White, J. J., et al. (2022). Phenotypic and mutational spectrum of ROR2-related Robinow syndrome. Human Mutation, 43( 7), 900-918. doi:10.1002/humu.24375
NLM
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Rosa ECCC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban–Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome [Internet]. Human Mutation. 2022 ; 43( 7): 900-918.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/humu.24375
Vancouver
Lima AR, Ferreira BM, Zhang C, Jolly A, Du H, White JJ, Dawood M, Lins TC, Chiabai MA, van Beusekom E, Cordoba MS, Rosa ECCC, Kayserili H, Kimonis V, Wu E, Mellado C, Aggarwal V, Richieri-Costa A, Brunoni D, Canó TM, Jorge AAL, Kim CA, Honjo R, Bertola DR, Dandalo-Girardi RM, Bayram Y, Gezdirici A, Yilmaz-Gulec E, Gumus E, Yilmaz GC, Okamoto N, Ohashi H, Coban–Akdemir Z, Mitani T, Jhangiani SN, Muzny DM, Regattieri NAP, Pogue R, Pereira RW, Otto PA, Gibbs RA, Ali BR, van Bokhoven H, Brunner HG, Sutton VR, Lupski JR, Vianna-Morgante AM, Carvalho CMB, Mazzeu JF. Phenotypic and mutational spectrum of ROR2-related Robinow syndrome [Internet]. Human Mutation. 2022 ; 43( 7): 900-918.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/humu.24375
Trabalho de evento-resumo
Fissuras raras da face e apêndices finger-like: desorganização em seres humanos (2022)
Serigatto, Henrique Regonaschi ; Virmond, Luiza do Amaral; Kokitsu-Nakata, Nancy Mizue ; Vendramini-Pittoli, Siulan ; Rosenberg, Carla ; Zechi-Ceide, Roseli Maria
Source: Anais. Conference titles: Congresso Médico Acadêmico de Bauru da Universidade de São Paulo - COMAB. Unidades: HRAC, IB, HRACF
Subjects: ANOMALIA FACIAL, TERATOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERIGATTO, Henrique Regonaschi et al. Fissuras raras da face e apêndices finger-like: desorganização em seres humanos. 2022, Anais.. Bauru: Faculdade de Odontologia de Bauru. Universidade de São Paulo, 2022. Disponível em: https://repositorio.usp.br/directbitstream/934b4ccb-9ab6-47a1-b2b4-0066de69de1c/3139253.pdf. Acesso em: 17 nov. 2024.
APA
Serigatto, H. R., Virmond, L. do A., Kokitsu-Nakata, N. M., Vendramini-Pittoli, S., Rosenberg, C., & Zechi-Ceide, R. M. (2022). Fissuras raras da face e apêndices finger-like: desorganização em seres humanos. In Anais. Bauru: Faculdade de Odontologia de Bauru. Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/934b4ccb-9ab6-47a1-b2b4-0066de69de1c/3139253.pdf
NLM
Serigatto HR, Virmond L do A, Kokitsu-Nakata NM, Vendramini-Pittoli S, Rosenberg C, Zechi-Ceide RM. Fissuras raras da face e apêndices finger-like: desorganização em seres humanos [Internet]. Anais. 2022 ;[citado 2024 nov. 17 ] Available from: https://repositorio.usp.br/directbitstream/934b4ccb-9ab6-47a1-b2b4-0066de69de1c/3139253.pdf
Vancouver
Serigatto HR, Virmond L do A, Kokitsu-Nakata NM, Vendramini-Pittoli S, Rosenberg C, Zechi-Ceide RM. Fissuras raras da face e apêndices finger-like: desorganização em seres humanos [Internet]. Anais. 2022 ;[citado 2024 nov. 17 ] Available from: https://repositorio.usp.br/directbitstream/934b4ccb-9ab6-47a1-b2b4-0066de69de1c/3139253.pdf
Trabalho de evento-resumo periodico
MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis (2022)
Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy Mizue; Alvarez, Camila Wenceslau ; Migliore, Chiara; Rafacho, Marina Bigeli ; Siemann, Maria Eugênia; Candido-Souza, Rosana Maria; Vendramini-Pittoli, Siulan; Tonello, Cristiano ; Maximino, Luciana Paula ; Meroni, Germana; Guion-Almeida, Maria Leine; Opitz, John M.; Richieri-Costa, Antonio
Source: European Journal of Human Genetics. Conference titles: European Society of Human Genetics. Unidades: HRAC, FOB, HRACF
Subjects: FISSURA LÁBIOPALATINA, HIPERTELORISMO, TRIAGEM, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZECHI-CEIDE, Roseli Maria et al. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis. European Journal of Human Genetics. London: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf. Acesso em: 17 nov. 2024. , 2022
APA
Zechi-Ceide, R. M., Kokitsu-Nakata, N. M., Alvarez, C. W., Migliore, C., Rafacho, M. B., Siemann, M. E., et al. (2022). MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis. European Journal of Human Genetics. London: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf
NLM
Zechi-Ceide RM, Kokitsu-Nakata NM, Alvarez CW, Migliore C, Rafacho MB, Siemann ME, Candido-Souza RM, Vendramini-Pittoli S, Tonello C, Maximino LP, Meroni G, Guion-Almeida ML, Opitz JM, Richieri-Costa A. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis [Internet]. European Journal of Human Genetics. 2022 ; 30 349-350.[citado 2024 nov. 17 ] Available from: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf
Vancouver
Zechi-Ceide RM, Kokitsu-Nakata NM, Alvarez CW, Migliore C, Rafacho MB, Siemann ME, Candido-Souza RM, Vendramini-Pittoli S, Tonello C, Maximino LP, Meroni G, Guion-Almeida ML, Opitz JM, Richieri-Costa A. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis [Internet]. European Journal of Human Genetics. 2022 ; 30 349-350.[citado 2024 nov. 17 ] Available from: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf
Artigo de periodico
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases (2022)
Vegas, Nancy ; Demir, Zeynep; Gordon, Christopher T.; Breton, Sylvain; Tavares, Vanessa Luiza Romanelli ; Moisset, Hugo; Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy M.; Kido, Yasuhiro; Marlin, Sandrine; Halem, Souad Gherbi; Meerschaut, Ilse; Callewaert, Bert; Chung, Brian ; Revencu, Nicole; Lehalle, Daphné; Petit, Florence ; Propst, Evan J.; Papsin, Blake C.; Phillips, John H.; Jakobsen, Linda; Tanno, Pauline Le; Thévenon, Julien; McGaughran, Julie; Gerkes, Erica H.; Leoni, Chiara; Kroisel, Peter; Tan, Tiong Y.; Henderson, Alex; Terhal, Paulien; Basel-Salmon, Lina; Alkindy, Adila; White, Susan M.; Passos-Bueno, Maria Rita ; Pingault, Véronique; Pontual, Loïc De; Amiel, Jeanne
Source: Human Mutation. Unidades: HRACF, HRAC, IB
Subjects: DOENÇAS MUSCULOSQUELÉTICAS, ANORMALIDADES CRANIOFACIAIS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VEGAS, Nancy et al. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, v. 43, n. 5, p. 582-594, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24349. Acesso em: 17 nov. 2024.
APA
Vegas, N., Demir, Z., Gordon, C. T., Breton, S., Tavares, V. L. R., Moisset, H., et al. (2022). Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, 43( 5), 582-594. doi:10.1002/humu.24349
NLM
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/humu.24349
Vancouver
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/humu.24349
Trabalho de evento-resumo
Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral (2021)
Ferraz, B. G.; Alonso, Nivaldo ; Brandão, Michele Madeira; Gomes, L. P.; Vendramini-Pittoli, Siulan
Source: Anais. Conference titles: JORMED - Jornada da Medicina USP Bauru. Unidades: FM, HRAC, FOB
Subjects: SÍNDROME DE GOLDENHAR, COLUNA VERTEBRAL, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, B. G. et al. Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral. 2021, Anais.. Macaé: CONGRESSE.ME, 2021. Disponível em: https://repositorio.usp.br/directbitstream/b47fde5b-623a-4fd7-a491-af9c0c30e972/3125092.pdf. Acesso em: 17 nov. 2024.
APA
Ferraz, B. G., Alonso, N., Brandão, M. M., Gomes, L. P., & Vendramini-Pittoli, S. (2021). Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral. In Anais. Macaé: CONGRESSE.ME. Recuperado de https://repositorio.usp.br/directbitstream/b47fde5b-623a-4fd7-a491-af9c0c30e972/3125092.pdf
NLM
Ferraz BG, Alonso N, Brandão MM, Gomes LP, Vendramini-Pittoli S. Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral [Internet]. Anais. 2021 ;[citado 2024 nov. 17 ] Available from: https://repositorio.usp.br/directbitstream/b47fde5b-623a-4fd7-a491-af9c0c30e972/3125092.pdf
Vancouver
Ferraz BG, Alonso N, Brandão MM, Gomes LP, Vendramini-Pittoli S. Morfologia da coluna vertebral de indivíduos com espectro oculoauriculo vertebral [Internet]. Anais. 2021 ;[citado 2024 nov. 17 ] Available from: https://repositorio.usp.br/directbitstream/b47fde5b-623a-4fd7-a491-af9c0c30e972/3125092.pdf
Artigo de periodico
A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects (2021)
Palagano, Eleonora; Gordon, Christopher T; Uva, Paolo ; Strina, Dario ; Dimartino, Clémantine; Villa, Anna; Amiel, Jeanne; Guion-Almeida, Maria Leine; Pittoli, Siulan Vendramini Paulovich ; Nakata, Nancy Mizue Kokitsu ; Zechi-Ceide, Roseli Maria ; Sobacchi, Cristina
Source: Bone. Unidade: HRAC
Subjects: DISOSTOSE MANDIBULOFACIAL, MUTAÇÃO GENÉTICA, FENÓTIPOS, CONVULSÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALAGANO, Eleonora et al. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects. Bone, v. 153, p. 7 , 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bone.2021.116152. Acesso em: 17 nov. 2024.
APA
Palagano, E., Gordon, C. T., Uva, P., Strina, D., Dimartino, C., Villa, A., et al. (2021). A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects. Bone, 153, 7 . doi:10.1016/j.bone.2021.116152
NLM
Palagano E, Gordon CT, Uva P, Strina D, Dimartino C, Villa A, Amiel J, Guion-Almeida ML, Pittoli SVP, Nakata NMK, Zechi-Ceide RM, Sobacchi C. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects [Internet]. Bone. 2021 ; 153 7 .[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bone.2021.116152
Vancouver
Palagano E, Gordon CT, Uva P, Strina D, Dimartino C, Villa A, Amiel J, Guion-Almeida ML, Pittoli SVP, Nakata NMK, Zechi-Ceide RM, Sobacchi C. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects [Internet]. Bone. 2021 ; 153 7 .[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bone.2021.116152
Artigo de periodico
Turner syndrome in diverse populations (2020)
Kruszka, Paul ; Addissie, Yonit A; Tekendo-Ngongang, Cedrik; Jones, Kelly L ; Savage, Sarah K.; Gupta, Neerja; Sirisena, Nirmala D; Dissanayake, Vajira H. W; Paththinige, C. Sampath; Aravena, Teresa; Nampoothiri, Sheela; Yesodharan, Dhanya; Girisha, Katta M ; Patil, Siddaramappa Jagdish ; Jamuar, Saumya Shekhar ; Goh, Jasmine Chew-Yin; Utari, Agustini ; Sihombing, Nydia; Mishra, Rupesh; Chitrakar, Neer Shoba; Iriele, Brenda C.; Lulseged, Ezana; Megarbane, Andre ; Uwineza, Annette; Oyenusi, Elizabeth Eberechi; Olopade, Oluwarotimi Bolaji; Fasanmade, Olufemi Adetola; Duenas-Roque, Milagros M.; Thong, Meow-Keong; Tung, Joanna Y. L; Mok, Gary T. K; Fleischer, Nicole; Rwegerera, Godfrey M; Herreros, María Beatriz; Watts, Johnathan; Fieggen, Karen; Huckstadt, Victoria; Moresco, Angélica; Obregon, María Gabriela; Hussen, Dalia Farouk; Ashaat, Neveen A ; Ashaat, Engy A. ; Chung, Brian H. Y; Badoe, Eben; Faradz, Sultana M. H; El Ruby, Mona O; Shotelersuk, Vorasuk; Wonkam, Ambroise; Ekure, Ekanem Nsikak; Phadke, Shubha R; Richieri-Costa, Antonio ; Muenke, Maximilian
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANÁLISE FACIAL, GENÉTICA DE POPULAÇÕES, FENÓTIPOS, ANORMALIDADES CONGÊNITAS, SÍNDROME DE NOONAN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KRUSZKA, Paul et al. Turner syndrome in diverse populations. American Journal of Medical Genetics. Part A, v. 182A, n. 2, p. 303-313, 2020Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61461. Acesso em: 17 nov. 2024.
APA
Kruszka, P., Addissie, Y. A., Tekendo-Ngongang, C., Jones, K. L., Savage, S. K., Gupta, N., et al. (2020). Turner syndrome in diverse populations. American Journal of Medical Genetics. Part A, 182A( 2), 303-313. doi:10.1002/ajmg.a.61461
NLM
Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC-Y, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong M-K, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Turner syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2020 ; 182A( 2): 303-313.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.61461
Vancouver
Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC-Y, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong M-K, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M. Turner syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2020 ; 182A( 2): 303-313.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.61461
Artigo de periodico
Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 (2020)
Pittoli, Siulan Vendramini Paulovich ; Souza, Rosana Maria Candido ; Quiezi, Rodrigo Gonçalves; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Jehee, Fernanda Sarquis; Ribeiro-Bicudo, Lucilene Arilho ; FitzPatrick, David R. ; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Journal of Pediatric Genetics. Unidades: HRAC, HRACF
Subjects: AGENESIA, FISSURA PALATINA, DELEÇÃO DE GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PITTOLI, Siulan Vendramini Paulovich et al. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2. Journal of Pediatric Genetics, v. 9, n. 4, p. 258-262, 2020Tradução . . Disponível em: https://doi.org/10.1055/s-0039-3402047. Acesso em: 17 nov. 2024.
APA
Pittoli, S. V. P., Souza, R. M. C., Quiezi, R. G., Zechi-Ceide, R. M., Nakata, N. M. K., Jehee, F. S., et al. (2020). Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2. Journal of Pediatric Genetics, 9( 4), 258-262. doi:10.1055/s-0039-3402047
NLM
Pittoli SVP, Souza RMC, Quiezi RG, Zechi-Ceide RM, Nakata NMK, Jehee FS, Ribeiro-Bicudo LA, FitzPatrick DR, Guion-Almeida ML, Richieri-Costa A. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 [Internet]. Journal of Pediatric Genetics. 2020 ; 9( 4): 258-262.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1055/s-0039-3402047
Vancouver
Pittoli SVP, Souza RMC, Quiezi RG, Zechi-Ceide RM, Nakata NMK, Jehee FS, Ribeiro-Bicudo LA, FitzPatrick DR, Guion-Almeida ML, Richieri-Costa A. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 [Internet]. Journal of Pediatric Genetics. 2020 ; 9( 4): 258-262.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1055/s-0039-3402047
Trabalho de evento-resumo
Submicroscopic chromosomal rearrangements in complex craniofacial syndromes (2019)
Souza, Rosana Maria Candido ; Zechi-Ceide, Roseli Maria ; Jehee, Fernanda Maria Sarquis; Richieri-Costa, Antonio
Source: Anais. Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas: A fronteira do conhecimento na reabilitação das anomalias craniofaciais. Unidades: HRAC, HRACF
Subjects: ANOMALIA CRANIOFACIAL, CROMOSSOMOS, ACONSELHAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Rosana Maria Candido et al. Submicroscopic chromosomal rearrangements in complex craniofacial syndromes. 2019, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2019. Disponível em: https://repositorio.usp.br/directbitstream/07fd33fc-2eab-467f-b5ba-4ef8e178054f/3193145.pdf. Acesso em: 17 nov. 2024.
APA
Souza, R. M. C., Zechi-Ceide, R. M., Jehee, F. M. S., & Richieri-Costa, A. (2019). Submicroscopic chromosomal rearrangements in complex craniofacial syndromes. In Anais. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/07fd33fc-2eab-467f-b5ba-4ef8e178054f/3193145.pdf
NLM
Souza RMC, Zechi-Ceide RM, Jehee FMS, Richieri-Costa A. Submicroscopic chromosomal rearrangements in complex craniofacial syndromes [Internet]. Anais. 2019 ;[citado 2024 nov. 17 ] Available from: https://repositorio.usp.br/directbitstream/07fd33fc-2eab-467f-b5ba-4ef8e178054f/3193145.pdf
Vancouver
Souza RMC, Zechi-Ceide RM, Jehee FMS, Richieri-Costa A. Submicroscopic chromosomal rearrangements in complex craniofacial syndromes [Internet]. Anais. 2019 ;[citado 2024 nov. 17 ] Available from: https://repositorio.usp.br/directbitstream/07fd33fc-2eab-467f-b5ba-4ef8e178054f/3193145.pdf
Artigo de periodico
Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome (2019)
Richieri-Costa, Antonio ; Zechi-Ceide, Roseli Maria ; Souza, Rosana Maria Candido ; Monteiro, Rejane Alves de Carvalho; Tonello, Cristiano; Freitas, Mariana L. de; Nakata, Nancy Mizue Kokitsu ; Pittoli, Siulan Vendramini Paulovich ; Mazzeu, Juliana F; Overes, Madelief; Ali-Amin, Roza; van Slegtenhorst, Marjon; Hoefsloot, Lies H; Jehee, Fernanda S
Source: American Journal of Medical Genetics. Unidades: HRAC, HRACF
Subjects: GENÉTICA, HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio et al. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, v. No 2019, n. 11, p. 2170-2177, 2019Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61305. Acesso em: 17 nov. 2024.
APA
Richieri-Costa, A., Zechi-Ceide, R. M., Souza, R. M. C., Monteiro, R. A. de C., Tonello, C., Freitas, M. L. de, et al. (2019). Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, No 2019( 11), 2170-2177. doi:10.1002/ajmg.a.61305
NLM
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.61305
Vancouver
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.61305
Artigo de periodico
Craniofacial morphology in patients with opitz G/BBB syndrome (2019)
Dalben, Gisele da Silva ; Garib, Daniela Gamba ; Pinto, Rayane de Oliveira ; Richieri-Costa, Antonio ; Taveira, Luís Antônio de Assis
Source: Cleft Palate-Craniofacial Journal. Unidades: HRAC, FOB
Subjects: CEFALOMETRIA, FISSURA LÁBIOPALATINA, ANOMALIA CRANIOFACIAL, MORFOLOGIA (ANATOMIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DALBEN, Gisele da Silva et al. Craniofacial morphology in patients with opitz G/BBB syndrome. Cleft Palate-Craniofacial Journal, v. no 2019, n. 10, p. 1366-1372, 2019Tradução . . Disponível em: https://doi.org/10.1177/1055665619857001. Acesso em: 17 nov. 2024.
APA
Dalben, G. da S., Garib, D. G., Pinto, R. de O., Richieri-Costa, A., & Taveira, L. A. de A. (2019). Craniofacial morphology in patients with opitz G/BBB syndrome. Cleft Palate-Craniofacial Journal, no 2019( 10), 1366-1372. doi:10.1177/1055665619857001
NLM
Dalben G da S, Garib DG, Pinto R de O, Richieri-Costa A, Taveira LA de A. Craniofacial morphology in patients with opitz G/BBB syndrome [Internet]. Cleft Palate-Craniofacial Journal. 2019 ; no 2019( 10): 1366-1372.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1177/1055665619857001
Vancouver
Dalben G da S, Garib DG, Pinto R de O, Richieri-Costa A, Taveira LA de A. Craniofacial morphology in patients with opitz G/BBB syndrome [Internet]. Cleft Palate-Craniofacial Journal. 2019 ; no 2019( 10): 1366-1372.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1177/1055665619857001

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