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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: 11 jun. 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 jun. 11 ] 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 jun. 11 ] Available from: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.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
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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: 11 jun. 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 jun. 11 ] 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 jun. 11 ] Available from: https://doi.org/10.1016/j.bone.2021.116152
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: 11 jun. 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 jun. 11 ] 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 jun. 11 ] Available from: https://doi.org/10.1055/s-0039-3402047
Artigo de periodico-carta/editorial
About Cuddapah et al.: Paper Entitled “IRF6 Sequencing in Interrupted Clefting” [Carta] (2017)
Alvarez, Camila Wenceslau ; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: The Cleft Palate Craniofacial Journal. Unidades: HRAC, HRACF
Subjects: FISSURA LÁBIOPALATINA, SEQUENCIAMENTO GENÉTICO, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVAREZ, Camila Wenceslau e GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. About Cuddapah et al.: Paper Entitled “IRF6 Sequencing in Interrupted Clefting” [Carta]. The Cleft Palate Craniofacial Journal. Thousand Oaks: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Disponível em: https://doi.org/10.1597/16-161. Acesso em: 11 jun. 2024. , 2017
APA
Alvarez, C. W., Guion-Almeida, M. L., & Richieri-Costa, A. (2017). About Cuddapah et al.: Paper Entitled “IRF6 Sequencing in Interrupted Clefting” [Carta]. The Cleft Palate Craniofacial Journal. Thousand Oaks: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. doi:10.1597/16-161
NLM
Alvarez CW, Guion-Almeida ML, Richieri-Costa A. About Cuddapah et al.: Paper Entitled “IRF6 Sequencing in Interrupted Clefting” [Carta] [Internet]. The Cleft Palate Craniofacial Journal. 2017 ; 54( 4): 494.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1597/16-161
Vancouver
Alvarez CW, Guion-Almeida ML, Richieri-Costa A. About Cuddapah et al.: Paper Entitled “IRF6 Sequencing in Interrupted Clefting” [Carta] [Internet]. The Cleft Palate Craniofacial Journal. 2017 ; 54( 4): 494.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1597/16-161
Trabalho de evento-resumo
Radiological and CT scan evaluation of mandible and ear in 56 cases with oculoaurivulovertebral spectrum (2015)
Pittoli, Siulan Vendramini Paulovich; Nakata, Nancy Mizue Kokitsu; Meira Júnior, Sílvio Garcia; Guion-Almeida, Maria Leine; Zechi-Ceide, Roseli Maria; Alvarez, Camila Wenceslau; Siqueira, Juliana de Alencar; Richieri-Costa, Antonio
Source: Final Program. Conference titles: European Craniofacial Congress. Unidade: HRAC
Subjects: ORELHA EXTERNA, DESENVOLVIMENTO CRANIOFACIAL, ANOMALIA CRANIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PITTOLI, Siulan Vendramini Paulovich et al. Radiological and CT scan evaluation of mandible and ear in 56 cases with oculoaurivulovertebral spectrum. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 11 jun. 2024.
APA
Pittoli, S. V. P., Nakata, N. M. K., Meira Júnior, S. G., Guion-Almeida, M. L., Zechi-Ceide, R. M., Alvarez, C. W., et al. (2015). Radiological and CT scan evaluation of mandible and ear in 56 cases with oculoaurivulovertebral spectrum. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index
NLM
Pittoli SVP, Nakata NMK, Meira Júnior SG, Guion-Almeida ML, Zechi-Ceide RM, Alvarez CW, Siqueira J de A, Richieri-Costa A. Radiological and CT scan evaluation of mandible and ear in 56 cases with oculoaurivulovertebral spectrum [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Vancouver
Pittoli SVP, Nakata NMK, Meira Júnior SG, Guion-Almeida ML, Zechi-Ceide RM, Alvarez CW, Siqueira J de A, Richieri-Costa A. Radiological and CT scan evaluation of mandible and ear in 56 cases with oculoaurivulovertebral spectrum [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Trabalho de evento-resumo
Phenotypic evaluation and evolution in syndromic (SC) and non-syndromic craniosynostosis (NSC): a retrospective study in 180 patients (2015)
Pittoli, Siulan Vendramini Paulovich; Nakata, Nancy Mizue Kokitsu; Guion-Almeida, Maria Leine; Zechi-Ceide, Roseli Maria; Alvarez, Camila Wenceslau; Richieri-Costa, Antonio
Source: Final Program. Conference titles: European Craniofacial Congress. Unidade: HRAC
Subjects: EVOLUÇÃO FENOTÍPICA, CRANIOSSINOSTOSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PITTOLI, Siulan Vendramini Paulovich et al. Phenotypic evaluation and evolution in syndromic (SC) and non-syndromic craniosynostosis (NSC): a retrospective study in 180 patients. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 11 jun. 2024.
APA
Pittoli, S. V. P., Nakata, N. M. K., Guion-Almeida, M. L., Zechi-Ceide, R. M., Alvarez, C. W., & Richieri-Costa, A. (2015). Phenotypic evaluation and evolution in syndromic (SC) and non-syndromic craniosynostosis (NSC): a retrospective study in 180 patients. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index
NLM
Pittoli SVP, Nakata NMK, Guion-Almeida ML, Zechi-Ceide RM, Alvarez CW, Richieri-Costa A. Phenotypic evaluation and evolution in syndromic (SC) and non-syndromic craniosynostosis (NSC): a retrospective study in 180 patients [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Vancouver
Pittoli SVP, Nakata NMK, Guion-Almeida ML, Zechi-Ceide RM, Alvarez CW, Richieri-Costa A. Phenotypic evaluation and evolution in syndromic (SC) and non-syndromic craniosynostosis (NSC): a retrospective study in 180 patients [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Trabalho de evento-resumo
Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP (2015)
Zechi-Ceide, Roseli Maria; Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu; Pittoli, Siulan Vendramini Paulovich
Source: Final Program. Conference titles: European Craniofacial Congress. Unidade: HRAC
Subjects: GENÉTICA, HOSPITAIS, SÍNDROME DE PIERRE ROBIN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZECHI-CEIDE, Roseli Maria et al. Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 11 jun. 2024.
APA
Zechi-Ceide, R. M., Guion-Almeida, M. L., Nakata, N. M. K., & Pittoli, S. V. P. (2015). Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index
NLM
Zechi-Ceide RM, Guion-Almeida ML, Nakata NMK, Pittoli SVP. Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Vancouver
Zechi-Ceide RM, Guion-Almeida ML, Nakata NMK, Pittoli SVP. Clinical genetic diagnostic and follow up of patients with Robin Sequence: an 13 years of experience at HRAC-USP [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Artigo de periodico
Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases (2015)
Verloes, Alain; Di Donato, Nataliya; Masliah-Planchon, Julien; Jongmans, Marjolijn; Abdul-Raman, Omar A.; Albrecht, Beate; Allanson, Judith; Brunnner, Han; Bertola, Débora; Chassaing, Nicolas; David, Albert; Devriendt, Koen; Eftekhari, Pirayeh; Drouin-Garraud, Valérie; Faravelli, Francesca; Faivre, Laurence; Giuliano, Fabienne; Guion-Almeida, Maria Leine; Juncos, Jorge; Kempers, Marlies; Eker, Hatice Koçak; Lacombe, Didier; Lin, Angela; Mancini, Grazia; Melis, Daniela; Lourenço, Charles Marques; Siu, Victoria Mok; Morin, Gilles; Nezarati, Marjan; Nowaczyk, Malgorzata J. M.; Ramer, Jeanette C.; Osimani, Sara; Philip, Nicole; Pierpont, Mary Ella; Procraccio, Vincent; Zechi-Ceide, Roseli Maria; Rossi, Massimiliano; Rusu, Cristina; Sznajer, Yves; Templin, Ludivine; Uliana, Vera; Klaus, Mirjam; Van Bon, Bregje; Van Ravenswaaij, Conny; Wainer, Bruce; Fry, Andrew E.; Rump, Andreas; Hoischen, Alexander; Drunat, Séverine; Rivière, Jean-Baptiste; Dobyns, William B.; Pilz, Daniela T.
Source: European Journal of Human Genetics. Unidade: HRAC
Subjects: GENÉTICA MÉDICA, ANORMALIDADES CRANIOFACIAIS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VERLOES, Alain et al. Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases. European Journal of Human Genetics, v. 23, n. 3, p. 292-301, 2015Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2014.95. Acesso em: 11 jun. 2024.
APA
Verloes, A., Di Donato, N., Masliah-Planchon, J., Jongmans, M., Abdul-Raman, O. A., Albrecht, B., et al. (2015). Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases. European Journal of Human Genetics, 23( 3), 292-301. doi:10.1038/ejhg.2014.95
NLM
Verloes A, Di Donato N, Masliah-Planchon J, Jongmans M, Abdul-Raman OA, Albrecht B, Allanson J, Brunnner H, Bertola D, Chassaing N, David A, Devriendt K, Eftekhari P, Drouin-Garraud V, Faravelli F, Faivre L, Giuliano F, Guion-Almeida ML, Juncos J, Kempers M, Eker HK, Lacombe D, Lin A, Mancini G, Melis D, Lourenço CM, Siu VM, Morin G, Nezarati M, Nowaczyk MJM, Ramer JC, Osimani S, Philip N, Pierpont ME, Procraccio V, Zechi-Ceide RM, Rossi M, Rusu C, Sznajer Y, Templin L, Uliana V, Klaus M, Van Bon B, Van Ravenswaaij C, Wainer B, Fry AE, Rump A, Hoischen A, Drunat S, Rivière J-B, Dobyns WB, Pilz DT. Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases [Internet]. European Journal of Human Genetics. 2015 ; 23( 3): 292-301.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1038/ejhg.2014.95
Vancouver
Verloes A, Di Donato N, Masliah-Planchon J, Jongmans M, Abdul-Raman OA, Albrecht B, Allanson J, Brunnner H, Bertola D, Chassaing N, David A, Devriendt K, Eftekhari P, Drouin-Garraud V, Faravelli F, Faivre L, Giuliano F, Guion-Almeida ML, Juncos J, Kempers M, Eker HK, Lacombe D, Lin A, Mancini G, Melis D, Lourenço CM, Siu VM, Morin G, Nezarati M, Nowaczyk MJM, Ramer JC, Osimani S, Philip N, Pierpont ME, Procraccio V, Zechi-Ceide RM, Rossi M, Rusu C, Sznajer Y, Templin L, Uliana V, Klaus M, Van Bon B, Van Ravenswaaij C, Wainer B, Fry AE, Rump A, Hoischen A, Drunat S, Rivière J-B, Dobyns WB, Pilz DT. Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases [Internet]. European Journal of Human Genetics. 2015 ; 23( 3): 292-301.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1038/ejhg.2014.95
Artigo de periodico
An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two cases (2015)
Pittoli, Siulan Vendramini Paulovich; Guion-Almeida, Maria Leine; Santos, J. M; Garcia Junior, Silvio Meira; Yoshida, Maurício Mitsuru; Richieri-Costa, Antonio; Nakata, Nancy Mizue Kokitsu
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PITTOLI, Siulan Vendramini Paulovich et al. An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two cases. Clinical Dysmorphology, v. 24, n. 4, p. 144-150, 2015Tradução . . Disponível em: https://doi.org/10.1097/mcd.0000000000000085. Acesso em: 11 jun. 2024.
APA
Pittoli, S. V. P., Guion-Almeida, M. L., Santos, J. M., Garcia Junior, S. M., Yoshida, M. M., Richieri-Costa, A., & Nakata, N. M. K. (2015). An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two cases. Clinical Dysmorphology, 24( 4), 144-150. doi:10.1097/mcd.0000000000000085
NLM
Pittoli SVP, Guion-Almeida ML, Santos JM, Garcia Junior SM, Yoshida MM, Richieri-Costa A, Nakata NMK. An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two cases [Internet]. Clinical Dysmorphology. 2015 ; 24( 4): 144-150.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1097/mcd.0000000000000085
Vancouver
Pittoli SVP, Guion-Almeida ML, Santos JM, Garcia Junior SM, Yoshida MM, Richieri-Costa A, Nakata NMK. An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two cases [Internet]. Clinical Dysmorphology. 2015 ; 24( 4): 144-150.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1097/mcd.0000000000000085
Trabalho de evento-resumo
Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients (2015)
Richieri-Costa, Antonio; Migliore, Chiara; Meroni, Germana; Siemann, Maria Eugênia; Zechi-Ceide, Roseli Maria; Nakata, Nancy Mizue Kokitsu; Pittoli, Siulan Vendramini Paulovich; Alvarez, Camila Wenceslau; Guion-Almeida, Maria Leine
Source: Final Program. Conference titles: European Craniofacial Congress. Unidade: HRAC
Subjects: GENÉTICA MÉDICA, HIPERTELORISMO, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio et al. Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 11 jun. 2024.
APA
Richieri-Costa, A., Migliore, C., Meroni, G., Siemann, M. E., Zechi-Ceide, R. M., Nakata, N. M. K., et al. (2015). Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index
NLM
Richieri-Costa A, Migliore C, Meroni G, Siemann ME, Zechi-Ceide RM, Nakata NMK, Pittoli SVP, Alvarez CW, Guion-Almeida ML. Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Vancouver
Richieri-Costa A, Migliore C, Meroni G, Siemann ME, Zechi-Ceide RM, Nakata NMK, Pittoli SVP, Alvarez CW, Guion-Almeida ML. Opitz G/BBB syndrome: clinical, imaging, and molecular findings in 15 brazilian patients [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Trabalho de evento-resumo
Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis (2015)
Alvarez, Camila Wenceslau; Guion-Almeida, Maria Leine; Rafacho, Marina Bigeli; Nakata, Nancy Mizue Kokitsu; Zechi-Ceide, Roseli Maria; Pittoli, Siulan Vendramini Paulovich; Meroni, Germana; Richieri-Costa, Antonio
Source: Final Program. Conference titles: European Craniofacial Congress. Unidade: HRAC
Subjects: EVOLUÇÃO FENOTÍPICA, FISSURA LÁBIOPALATINA, HIPERTELORISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVAREZ, Camila Wenceslau et al. Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 11 jun. 2024.
APA
Alvarez, C. W., Guion-Almeida, M. L., Rafacho, M. B., Nakata, N. M. K., Zechi-Ceide, R. M., Pittoli, S. V. P., et al. (2015). Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index
NLM
Alvarez CW, Guion-Almeida ML, Rafacho MB, Nakata NMK, Zechi-Ceide RM, Pittoli SVP, Meroni G, Richieri-Costa A. Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Vancouver
Alvarez CW, Guion-Almeida ML, Rafacho MB, Nakata NMK, Zechi-Ceide RM, Pittoli SVP, Meroni G, Richieri-Costa A. Phenotypic evolution in Optiz GBBB Syndrome: clues for diagnosis and prognosis [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Artigo de periodico
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia (2015)
Gordon, Christopher T; Weaver, K. Nicole; Zechi-Ceide, Roseli Maria ; Madsen, Erik C.; Tavares, Andre L. P.; Oufadem, Myriam; Kurihara, Yukiko; Adameyko, Igor; Picard, Arnaud ; Breton, Sylvain; Pierrot, Sébastien; Biosse-Duplan, Martin; Voisin, Norine; Masson, Cécile; Bole-Feysot, Christine; Nitschké, Patrick; Delrue, Marie-Ange; Lacombe, Didier; Guion-Almeida, Maria Leine; Moura, Priscila Padilha; Garib, Daniela Gamba ; Munnich, Arnold; Ernfors, Patrik; Hufnagel, Robert B.; Hopkin, Robert J.
Source: American Journal of Human Genetics. Unidades: HRAC, FOB
Subjects: ALOPECIA, DISOSTOSE MANDIBULOFACIAL, MUTAÇÃO GENÉTICA, TOMOGRAFIA COMPUTADORIZADA POR RAIOS X
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GORDON, Christopher T et al. Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia. American Journal of Human Genetics, v. 96, n. 4, p. 519-531, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2015.01.015. Acesso em: 11 jun. 2024.
APA
Gordon, C. T., Weaver, K. N., Zechi-Ceide, R. M., Madsen, E. C., Tavares, A. L. P., Oufadem, M., et al. (2015). Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia. American Journal of Human Genetics, 96( 4), 519-531. doi:10.1016/j.ajhg.2015.01.015
NLM
Gordon CT, Weaver KN, Zechi-Ceide RM, Madsen EC, Tavares ALP, Oufadem M, Kurihara Y, Adameyko I, Picard A, Breton S, Pierrot S, Biosse-Duplan M, Voisin N, Masson C, Bole-Feysot C, Nitschké P, Delrue M-A, Lacombe D, Guion-Almeida ML, Moura PP, Garib DG, Munnich A, Ernfors P, Hufnagel RB, Hopkin RJ. Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia [Internet]. American Journal of Human Genetics. 2015 ; 96( 4): 519-531.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1016/j.ajhg.2015.01.015
Vancouver
Gordon CT, Weaver KN, Zechi-Ceide RM, Madsen EC, Tavares ALP, Oufadem M, Kurihara Y, Adameyko I, Picard A, Breton S, Pierrot S, Biosse-Duplan M, Voisin N, Masson C, Bole-Feysot C, Nitschké P, Delrue M-A, Lacombe D, Guion-Almeida ML, Moura PP, Garib DG, Munnich A, Ernfors P, Hufnagel RB, Hopkin RJ. Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia [Internet]. American Journal of Human Genetics. 2015 ; 96( 4): 519-531.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1016/j.ajhg.2015.01.015
Trabalho de evento-resumo
Three-dimensional analysis of the mandible and the zygomatic arch of seven brazilian patients with mandibulofacial dysostosis (2015)
Moura, Priscila Padilha; Peixoto, Adriano Porto; Garib, Daniela Gamba; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio; Zechi-Ceide, Roseli Maria
Source: Final Program. Conference titles: European Craniofacial Congress. Unidades: HRAC, FOB
Subjects: DISOSTOSE MANDIBULOFACIAL, TERCEIRA DIMENSÃO, GENÉTICA MÉDICA
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ABNT
MOURA, Priscila Padilha et al. Three-dimensional analysis of the mandible and the zygomatic arch of seven brazilian patients with mandibulofacial dysostosis. 2015, Anais.. Gothenburg: European Cleft Plate and Craniofacial Association, 2015. Disponível em: http://www.ecc2015.se/author-index. Acesso em: 11 jun. 2024.
APA
Moura, P. P., Peixoto, A. P., Garib, D. G., Guion-Almeida, M. L., Richieri-Costa, A., & Zechi-Ceide, R. M. (2015). Three-dimensional analysis of the mandible and the zygomatic arch of seven brazilian patients with mandibulofacial dysostosis. In Final Program. Gothenburg: European Cleft Plate and Craniofacial Association. Recuperado de http://www.ecc2015.se/author-index
NLM
Moura PP, Peixoto AP, Garib DG, Guion-Almeida ML, Richieri-Costa A, Zechi-Ceide RM. Three-dimensional analysis of the mandible and the zygomatic arch of seven brazilian patients with mandibulofacial dysostosis [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Vancouver
Moura PP, Peixoto AP, Garib DG, Guion-Almeida ML, Richieri-Costa A, Zechi-Ceide RM. Three-dimensional analysis of the mandible and the zygomatic arch of seven brazilian patients with mandibulofacial dysostosis [Internet]. Final Program. 2015 ;[citado 2024 jun. 11 ] Available from: http://www.ecc2015.se/author-index
Artigo de periodico
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect (2015)
Tavares, Vanessa Luiza Romanelli ; Gordon, Christopher T; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Voisin, Norine; Tan, Tiong Y; Heggie, Andrew A; Pittoli, Siulan Vendramini Paulovich ; Propst, Evan J; Papsin, Blake C; Torres, Tatiana Teixeira ; Buermans, Henk; Capelo, Luciane Portas; Den Dunnen, Johan T; Guion-Almeida, Maria Leine; Lyonnet, Stanislas; Amiel, Jeanne; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Unidades: HRAC, IB
Subjects: ANORMALIDADES CRANIOFACIAIS, DOENÇAS GENÉTICAS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAVARES, Vanessa Luiza Romanelli et al. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect. European Journal of Human Genetics, v. 23, n. 4, p. 481-485, 2015Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2014.132. Acesso em: 11 jun. 2024.
APA
Tavares, V. L. R., Gordon, C. T., Zechi-Ceide, R. M., Nakata, N. M. K., Voisin, N., Tan, T. Y., et al. (2015). Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect. European Journal of Human Genetics, 23( 4), 481-485. doi:10.1038/ejhg.2014.132
NLM
Tavares VLR, Gordon CT, Zechi-Ceide RM, Nakata NMK, Voisin N, Tan TY, Heggie AA, Pittoli SVP, Propst EJ, Papsin BC, Torres TT, Buermans H, Capelo LP, Den Dunnen JT, Guion-Almeida ML, Lyonnet S, Amiel J, Passos-Bueno MR. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect [Internet]. European Journal of Human Genetics. 2015 ; 23( 4): 481-485.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Vancouver
Tavares VLR, Gordon CT, Zechi-Ceide RM, Nakata NMK, Voisin N, Tan TY, Heggie AA, Pittoli SVP, Propst EJ, Papsin BC, Torres TT, Buermans H, Capelo LP, Den Dunnen JT, Guion-Almeida ML, Lyonnet S, Amiel J, Passos-Bueno MR. Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect [Internet]. European Journal of Human Genetics. 2015 ; 23( 4): 481-485.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Artigo de periodico
Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement (2014)
Alvarez, Camila Wenceslau ; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Journal of Cranio-Maxillo-Facial Surgery. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, FENÓTIPOS, REBORDO ALVEOLAR
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ABNT
ALVAREZ, Camila Wenceslau e GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement. Journal of Cranio-Maxillo-Facial Surgery, v. 42, n. 8, p. 1952-1957, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.jcms.2014.08.007. Acesso em: 11 jun. 2024.
APA
Alvarez, C. W., Guion-Almeida, M. L., & Richieri-Costa, A. (2014). Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement. Journal of Cranio-Maxillo-Facial Surgery, 42( 8), 1952-1957. doi:10.1016/j.jcms.2014.08.007
NLM
Alvarez CW, Guion-Almeida ML, Richieri-Costa A. Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement [Internet]. Journal of Cranio-Maxillo-Facial Surgery. 2014 ; 42( 8): 1952-1957.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1016/j.jcms.2014.08.007
Vancouver
Alvarez CW, Guion-Almeida ML, Richieri-Costa A. Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement [Internet]. Journal of Cranio-Maxillo-Facial Surgery. 2014 ; 42( 8): 1952-1957.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1016/j.jcms.2014.08.007
Trabalho de evento-resumo
Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding (2014)
Tavares, Vanessa Luiza; Gordon, Christhofer T.; Torres, T.; Voisin, N.; Bertola, D.; Ceide, Roseli Maria Zechi; Tan, T. Y.; Heggie, A. A. C.; Propst, E.; Papsin, B. C.; Nakata, Nancy Mizue Kokitsu; Guion-Almeida, Maria Leine; Pittoli, Siulan Vendramini Pailovich; Lyonnet, Stanislas; Amiel, Jeanne; Passos-Bueno, Maria Rita
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, MALFORMAÇÕES, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TAVARES, Vanessa Luiza et al. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. 2014, Anais.. Milan: ESHG, 2014. . Acesso em: 11 jun. 2024.
APA
Tavares, V. L., Gordon, C. T., Torres, T., Voisin, N., Bertola, D., Ceide, R. M. Z., et al. (2014). Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. In Abstracts. Milan: ESHG.
NLM
Tavares VL, Gordon CT, Torres T, Voisin N, Bertola D, Ceide RMZ, Tan TY, Heggie AAC, Propst E, Papsin BC, Nakata NMK, Guion-Almeida ML, Pittoli SVP, Lyonnet S, Amiel J, Passos-Bueno MR. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. Abstracts. 2014 ;[citado 2024 jun. 11 ]
Vancouver
Tavares VL, Gordon CT, Torres T, Voisin N, Bertola D, Ceide RMZ, Tan TY, Heggie AAC, Propst E, Papsin BC, Nakata NMK, Guion-Almeida ML, Pittoli SVP, Lyonnet S, Amiel J, Passos-Bueno MR. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. Abstracts. 2014 ;[citado 2024 jun. 11 ]
Artigo de periodico
Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome (2014)
Gordon, Christopher T.; Cunniff, Christopher M.; Green, Glenn E.; Zechi-Ceide, Roseli Maria ; Johnson, Jason M.; Henderson, Alex; Petit, Florence; Nakata, Nancy Mizue Kokitsu ; Guion-Almeida, Maria Leine; Munnich, Arnold; Cunningham, Michael L.; Lyonnet, Stanislas; Amiel, Jeanne
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: DESENVOLVIMENTO MAXILOFACIAL, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GORDON, Christopher T. et al. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome. American Journal of Medical Genetics Part A, v. 164, n. 7, p. 1850-1853, 2014Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36505. Acesso em: 11 jun. 2024.
APA
Gordon, C. T., Cunniff, C. M., Green, G. E., Zechi-Ceide, R. M., Johnson, J. M., Henderson, A., et al. (2014). Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome. American Journal of Medical Genetics Part A, 164( 7), 1850-1853. doi:10.1002/ajmg.a.36505
NLM
Gordon CT, Cunniff CM, Green GE, Zechi-Ceide RM, Johnson JM, Henderson A, Petit F, Nakata NMK, Guion-Almeida ML, Munnich A, Cunningham ML, Lyonnet S, Amiel J. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 164( 7): 1850-1853.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Vancouver
Gordon CT, Cunniff CM, Green GE, Zechi-Ceide RM, Johnson JM, Henderson A, Petit F, Nakata NMK, Guion-Almeida ML, Munnich A, Cunningham ML, Lyonnet S, Amiel J. Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome [Internet]. American Journal of Medical Genetics Part A. 2014 ; 164( 7): 1850-1853.[citado 2024 jun. 11 ] Available from: https://doi.org/10.1002/ajmg.a.36505
Trabalho de evento-resumo
Investigação radiológica e tomográfica da mandíbula de indivíduos com anomalias de 1º e 2º arcos faríngeos (2014)
Pittoli, Siulan Vendramini Pailovich; Nakata, Nancy Mizue Kokitsu; Santos, Juliana Mercado; Garcia Junior, Silvio Meira; Richieri-Costa, Antonio; Guion-Almeida, Maria Leine
Source: Anais. Conference titles: Congresso Brasileiro de Genética Médica. Unidade: HRAC
Subjects: ANOMALIA CRANIOFACIAL, MALFORMAÇÕES, ORELHA EXTERNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PITTOLI, Siulan Vendramini Pailovich et al. Investigação radiológica e tomográfica da mandíbula de indivíduos com anomalias de 1º e 2º arcos faríngeos. 2014, Anais.. Fortaleza: Sociedade Brasileira de Genética Médica (SBGM), 2014. . Acesso em: 11 jun. 2024.
APA
Pittoli, S. V. P., Nakata, N. M. K., Santos, J. M., Garcia Junior, S. M., Richieri-Costa, A., & Guion-Almeida, M. L. (2014). Investigação radiológica e tomográfica da mandíbula de indivíduos com anomalias de 1º e 2º arcos faríngeos. In Anais. Fortaleza: Sociedade Brasileira de Genética Médica (SBGM).
NLM
Pittoli SVP, Nakata NMK, Santos JM, Garcia Junior SM, Richieri-Costa A, Guion-Almeida ML. Investigação radiológica e tomográfica da mandíbula de indivíduos com anomalias de 1º e 2º arcos faríngeos. Anais. 2014 ;[citado 2024 jun. 11 ]
Vancouver
Pittoli SVP, Nakata NMK, Santos JM, Garcia Junior SM, Richieri-Costa A, Guion-Almeida ML. Investigação radiológica e tomográfica da mandíbula de indivíduos com anomalias de 1º e 2º arcos faríngeos. Anais. 2014 ;[citado 2024 jun. 11 ]
Trabalho de evento
Genética clínica (2014)
Richieri-Costa, Antonio ; Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu ; Zechi-Ceide, Roseli Maria ; Pittoli, Siulan Vendramini Paulovich ; Alvarez, Camila Wenceslau
Source: Anais. Conference titles: Curso de Anomalias Congênitas Labiopalatinas. Unidade: HRAC
Subjects: GENÉTICA, ANORMALIDADES CRANIOFACIAIS, HOSPITAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio et al. Genética clínica. 2014, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2014. Disponível em: https://repositorio.usp.br/directbitstream/4902fe1a-05e7-407b-8e0b-40ffcee0dbbd/2514126.pdf. Acesso em: 11 jun. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., Nakata, N. M. K., Zechi-Ceide, R. M., Pittoli, S. V. P., & Alvarez, C. W. (2014). Genética clínica. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/4902fe1a-05e7-407b-8e0b-40ffcee0dbbd/2514126.pdf
NLM
Richieri-Costa A, Guion-Almeida ML, Nakata NMK, Zechi-Ceide RM, Pittoli SVP, Alvarez CW. Genética clínica [Internet]. Anais. 2014 ;[citado 2024 jun. 11 ] Available from: https://repositorio.usp.br/directbitstream/4902fe1a-05e7-407b-8e0b-40ffcee0dbbd/2514126.pdf
Vancouver
Richieri-Costa A, Guion-Almeida ML, Nakata NMK, Zechi-Ceide RM, Pittoli SVP, Alvarez CW. Genética clínica [Internet]. Anais. 2014 ;[citado 2024 jun. 11 ] Available from: https://repositorio.usp.br/directbitstream/4902fe1a-05e7-407b-8e0b-40ffcee0dbbd/2514126.pdf
Trabalho de evento-resumo
Espectro oculoauriculovertebral com fissura tessier 30. Relato de dois casos (2014)
Nakata, Nancy Mizue Kokitsu; Guion-Almeida, Maria Leine; Santos, Juliana Mercado; Garcia Junior, Silvio Meira; Yoshida, Maurício Mitsuru; Richieri-Costa, Antonio; Pittoli, Siulan Vendramini Pailovich
Source: Anais. Conference titles: Congresso Brasileiro de Genética Médica. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, ANOMALIA CRANIOFACIAL, FENÓTIPOS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu et al. Espectro oculoauriculovertebral com fissura tessier 30. Relato de dois casos. 2014, Anais.. Fortaleza: Sociedade Brasileira de Genética Médica (SBGM), 2014. . Acesso em: 11 jun. 2024.
APA
Nakata, N. M. K., Guion-Almeida, M. L., Santos, J. M., Garcia Junior, S. M., Yoshida, M. M., Richieri-Costa, A., & Pittoli, S. V. P. (2014). Espectro oculoauriculovertebral com fissura tessier 30. Relato de dois casos. In Anais. Fortaleza: Sociedade Brasileira de Genética Médica (SBGM).
NLM
Nakata NMK, Guion-Almeida ML, Santos JM, Garcia Junior SM, Yoshida MM, Richieri-Costa A, Pittoli SVP. Espectro oculoauriculovertebral com fissura tessier 30. Relato de dois casos. Anais. 2014 ;[citado 2024 jun. 11 ]
Vancouver
Nakata NMK, Guion-Almeida ML, Santos JM, Garcia Junior SM, Yoshida MM, Richieri-Costa A, Pittoli SVP. Espectro oculoauriculovertebral com fissura tessier 30. Relato de dois casos. Anais. 2014 ;[citado 2024 jun. 11 ]

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