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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, HRACF
Subjects: MICROGNATISMO, FOTOGRAFIA, SÍNDROME DE PIERRE ROBIN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 02 jun. 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 jun. 02 ] 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 jun. 02 ] Available from: http://dx.doi.org/10.1097/SCS.0000000000009749
Artigo de periodico
Stress induced phosphoprotein 1 overexpression controls proliferation, migration and invasion and is associated with poor survival in oral squamous cell carcinoma (2023)
Dourado, Mauricio Rocha ; Elseragy, Amr; Costa, Bruno Cesar da; Téo, Fábio Haach; Guimarães, Gustavo Narvaes; Machado, Renato Assis ; Risteli, Maija; Wahbi, Wafa; Rocha, Clarissa Araújo Gurgel; Paranaíba, Lívia Máris Ribeiro ; González-Arriagada, Wilfredo Alejandro ; Silva, Sabrina Daniela da; Rangel, Ana Lúcia Carrinho Ayroza ; Marques, Marcelo Rocha; Rossa Junior, Carlos ; Salo, Tuula; Coletta, Ricardo D.
Unidade: HRAC
Subjects: NEOPLASIAS BUCAIS, CARCINOMA DE CÉLULAS ESCAMOSAS, PROGNÓSTICO, PROLIFERAÇÃO CELULAR, METÁSTASE NEOPLÁSICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DOURADO, Mauricio Rocha et al. Stress induced phosphoprotein 1 overexpression controls proliferation, migration and invasion and is associated with poor survival in oral squamous cell carcinoma. v. 12, n. 1, 2023Tradução . . Disponível em: https://doi.org/10.3389/fonc.2022.1085917. Acesso em: 02 jun. 2024.
APA
Dourado, M. R., Elseragy, A., Costa, B. C. da, Téo, F. H., Guimarães, G. N., Machado, R. A., et al. (2023). Stress induced phosphoprotein 1 overexpression controls proliferation, migration and invasion and is associated with poor survival in oral squamous cell carcinoma, 12( 1). doi:10.3389/fonc.2022.1085917
NLM
Dourado MR, Elseragy A, Costa BC da, Téo FH, Guimarães GN, Machado RA, Risteli M, Wahbi W, Rocha CAG, Paranaíba LMR, González-Arriagada WA, Silva SD da, Rangel ALCA, Marques MR, Rossa Junior C, Salo T, Coletta RD. Stress induced phosphoprotein 1 overexpression controls proliferation, migration and invasion and is associated with poor survival in oral squamous cell carcinoma [Internet]. 2023 ; 12( 1):[citado 2024 jun. 02 ] Available from: https://doi.org/10.3389/fonc.2022.1085917
Vancouver
Dourado MR, Elseragy A, Costa BC da, Téo FH, Guimarães GN, Machado RA, Risteli M, Wahbi W, Rocha CAG, Paranaíba LMR, González-Arriagada WA, Silva SD da, Rangel ALCA, Marques MR, Rossa Junior C, Salo T, Coletta RD. Stress induced phosphoprotein 1 overexpression controls proliferation, migration and invasion and is associated with poor survival in oral squamous cell carcinoma [Internet]. 2023 ; 12( 1):[citado 2024 jun. 02 ] Available from: https://doi.org/10.3389/fonc.2022.1085917
Artigo de periodico
Effects of sequential bilateral cochlear implantation in children: evidence from speech-evoked cortical potentials and tests of speech perception (2022)
Vicente, Leticia Cristina; Polonenko, Melissa Jane ; Gordon, Karen Ann; Silva, Leandra Tabanez do Nascimento ; Costa, Orozimbo Alves da ; Alvarenga, Kátia de Freitas
Source: Audiology & Neuro-Otology. Unidades: HRAC, FOB
Subjects: AUDIÇÃO, PERCEPÇÃO AUDITIVA, PERCEPÇÃO DA FALA, CRIANÇAS, IMPLANTE DA CÓCLEA, POTENCIAIS EVOCADOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VICENTE, Leticia Cristina et al. Effects of sequential bilateral cochlear implantation in children: evidence from speech-evoked cortical potentials and tests of speech perception. Audiology & Neuro-Otology, v. 27, n. 4, p. 282-296, 2022Tradução . . Disponível em: https://doi.org/10.1159/000521600. Acesso em: 02 jun. 2024.
APA
Vicente, L. C., Polonenko, M. J., Gordon, K. A., Silva, L. T. do N., Costa, O. A. da, & Alvarenga, K. de F. (2022). Effects of sequential bilateral cochlear implantation in children: evidence from speech-evoked cortical potentials and tests of speech perception. Audiology & Neuro-Otology, 27( 4), 282-296. doi:10.1159/000521600
NLM
Vicente LC, Polonenko MJ, Gordon KA, Silva LT do N, Costa OA da, Alvarenga K de F. Effects of sequential bilateral cochlear implantation in children: evidence from speech-evoked cortical potentials and tests of speech perception [Internet]. Audiology & Neuro-Otology. 2022 ; 27( 4): 282-296.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1159/000521600
Vancouver
Vicente LC, Polonenko MJ, Gordon KA, Silva LT do N, Costa OA da, Alvarenga K de F. Effects of sequential bilateral cochlear implantation in children: evidence from speech-evoked cortical potentials and tests of speech perception [Internet]. Audiology & Neuro-Otology. 2022 ; 27( 4): 282-296.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1159/000521600
Artigo de periodico
Trophoblast cell surface antigen 2 expression predicts outcome in oral squamous cell carcinomas (2022)
Dourado, Mauricio Rocha ; Machado, Renato Assis ; Paranaíba, Lívia Máris Ribeiro ; González-Arriagada, Wilfredo Alejandro ; Silva, Sabrina Daniela da; Sawazaki-Calone, Íris; Graner, Edgard ; Salo, Tuula; Coletta, Ricardo D.
Source: Oral Diseases. Unidade: HRAC
Subjects: CARCINOMA DE CÉLULAS ESCAMOSAS, SOBREVIDA, TROFOBLASTO, ANTÍGENOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DOURADO, Mauricio Rocha et al. Trophoblast cell surface antigen 2 expression predicts outcome in oral squamous cell carcinomas. Oral Diseases, v. 28, n. 4, p. 1085-1093, 2022Tradução . . Disponível em: https://doi.org/10.1111/odi.13809. Acesso em: 02 jun. 2024.
APA
Dourado, M. R., Machado, R. A., Paranaíba, L. M. R., González-Arriagada, W. A., Silva, S. D. da, Sawazaki-Calone, Í., et al. (2022). Trophoblast cell surface antigen 2 expression predicts outcome in oral squamous cell carcinomas. Oral Diseases, 28( 4), 1085-1093. doi:10.1111/odi.13809
NLM
Dourado MR, Machado RA, Paranaíba LMR, González-Arriagada WA, Silva SD da, Sawazaki-Calone Í, Graner E, Salo T, Coletta RD. Trophoblast cell surface antigen 2 expression predicts outcome in oral squamous cell carcinomas [Internet]. Oral Diseases. 2022 ; 28( 4): 1085-1093.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1111/odi.13809
Vancouver
Dourado MR, Machado RA, Paranaíba LMR, González-Arriagada WA, Silva SD da, Sawazaki-Calone Í, Graner E, Salo T, Coletta RD. Trophoblast cell surface antigen 2 expression predicts outcome in oral squamous cell carcinomas [Internet]. Oral Diseases. 2022 ; 28( 4): 1085-1093.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1111/odi.13809
Artigo de periodico
A cleft-customized occlusal rating system to assess orthodontic occlusal improvement in patients with unilateral cleft lip and palate (2022)
Pinheiro, Fábio Henrique de Sá Leitão; Frota, Carolina Martins ; Garib, Daniela Gamba ; Sathler-Zanda, Renata ; Ozawa, Terumi Okada ; Lauris, Rita de Cássia Moura Carvalho ; Kato, Renata Mayumi ; Kurimori, Érika Tiemi
Source: The Cleft Palate-Craniofacial Journal. Unidades: FOB, HRAC, HRACF
Subjects: OCLUSÃO DENTÁRIA, ARCADA DENTÁRIA, FISSURA LÁBIOPALATINA, ORTODONTIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINHEIRO, Fábio Henrique de Sá Leitão et al. A cleft-customized occlusal rating system to assess orthodontic occlusal improvement in patients with unilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal, v. 59, n. Ja 2022, p. 54-65, 2022Tradução . . Disponível em: https://doi.org/10.1177/1055665621995313. Acesso em: 02 jun. 2024.
APA
Pinheiro, F. H. de S. L., Frota, C. M., Garib, D. G., Sathler-Zanda, R., Ozawa, T. O., Lauris, R. de C. M. C., et al. (2022). A cleft-customized occlusal rating system to assess orthodontic occlusal improvement in patients with unilateral cleft lip and palate. The Cleft Palate-Craniofacial Journal, 59( Ja 2022), 54-65. doi:10.1177/1055665621995313
NLM
Pinheiro FH de SL, Frota CM, Garib DG, Sathler-Zanda R, Ozawa TO, Lauris R de CMC, Kato RM, Kurimori ÉT. A cleft-customized occlusal rating system to assess orthodontic occlusal improvement in patients with unilateral cleft lip and palate [Internet]. The Cleft Palate-Craniofacial Journal. 2022 ; 59( Ja 2022): 54-65.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1177/1055665621995313
Vancouver
Pinheiro FH de SL, Frota CM, Garib DG, Sathler-Zanda R, Ozawa TO, Lauris R de CMC, Kato RM, Kurimori ÉT. A cleft-customized occlusal rating system to assess orthodontic occlusal improvement in patients with unilateral cleft lip and palate [Internet]. The Cleft Palate-Craniofacial Journal. 2022 ; 59( Ja 2022): 54-65.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1177/1055665621995313
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: 02 jun. 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 jun. 02 ] 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 jun. 02 ] Available from: https://doi.org/10.1002/humu.24349
Artigo de periodico
Interdisciplinary treatment of patients with cleidocranial dysplasia and multiple unerupted permanent teeth (2021)
Frota, Carolina Martins ; Pinheiro, Fábio Henrique de Sá Leitão; Caetano, Isabela Maria; Carvalho, Roberta Martinelli; Aiello, Carlos Alberto
Source: Journal of Clinical Orthodontics. Unidade: HRAC
Subjects: DISPLASIA CLEIDOCRANIANA, DENTE NÃO ERUPCIONADO, DENTE PERMANENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FROTA, Carolina Martins et al. Interdisciplinary treatment of patients with cleidocranial dysplasia and multiple unerupted permanent teeth. Journal of Clinical Orthodontics, v. No 2021, n. 11, p. 1-13, 2021Tradução . . Disponível em: https://www.jco-online.com/archive/2021/11/20211101-interdisciplinary-treatment-of-patients-with-cleidocranial-dysplasia-and-multiple-unerupted-permanent-teeth/. Acesso em: 02 jun. 2024.
APA
Frota, C. M., Pinheiro, F. H. de S. L., Caetano, I. M., Carvalho, R. M., & Aiello, C. A. (2021). Interdisciplinary treatment of patients with cleidocranial dysplasia and multiple unerupted permanent teeth. Journal of Clinical Orthodontics, No 2021( 11), 1-13. Recuperado de https://www.jco-online.com/archive/2021/11/20211101-interdisciplinary-treatment-of-patients-with-cleidocranial-dysplasia-and-multiple-unerupted-permanent-teeth/
NLM
Frota CM, Pinheiro FH de SL, Caetano IM, Carvalho RM, Aiello CA. Interdisciplinary treatment of patients with cleidocranial dysplasia and multiple unerupted permanent teeth [Internet]. Journal of Clinical Orthodontics. 2021 ; No 2021( 11): 1-13.[citado 2024 jun. 02 ] Available from: https://www.jco-online.com/archive/2021/11/20211101-interdisciplinary-treatment-of-patients-with-cleidocranial-dysplasia-and-multiple-unerupted-permanent-teeth/
Vancouver
Frota CM, Pinheiro FH de SL, Caetano IM, Carvalho RM, Aiello CA. Interdisciplinary treatment of patients with cleidocranial dysplasia and multiple unerupted permanent teeth [Internet]. Journal of Clinical Orthodontics. 2021 ; No 2021( 11): 1-13.[citado 2024 jun. 02 ] Available from: https://www.jco-online.com/archive/2021/11/20211101-interdisciplinary-treatment-of-patients-with-cleidocranial-dysplasia-and-multiple-unerupted-permanent-teeth/
Trabalho de evento-resumo
Self-perception of dentofacial esthetics in individuals with cleft lip and palate (2019)
Frota, Carolina Martins ; Garib, Daniela Gamba ; Pinheiro, Fábio Henrique de Sá Leitão; Sathler, Renata Carvalho
Source: Anais. Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas: A fronteira do conhecimento na reabilitação das anomalias craniofaciais. Unidades: FOB, HRAC, HRACF
Subjects: AUTOPERCEPÇÃO, FISSURA LÁBIOPALATINA, ESTÉTICA DENTÁRIA, TRATAMENTO ORTODÔNTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FROTA, Carolina Martins et al. Self-perception of dentofacial esthetics in individuals with cleft lip and palate. 2019, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2019. Disponível em: https://repositorio.usp.br/directbitstream/3a830143-a19c-4b97-96c6-ac488f6f4980/3193422.pdf. Acesso em: 02 jun. 2024.
APA
Frota, C. M., Garib, D. G., Pinheiro, F. H. de S. L., & Sathler, R. C. (2019). Self-perception of dentofacial esthetics in individuals with cleft lip and palate. In Anais. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/3a830143-a19c-4b97-96c6-ac488f6f4980/3193422.pdf
NLM
Frota CM, Garib DG, Pinheiro FH de SL, Sathler RC. Self-perception of dentofacial esthetics in individuals with cleft lip and palate [Internet]. Anais. 2019 ;[citado 2024 jun. 02 ] Available from: https://repositorio.usp.br/directbitstream/3a830143-a19c-4b97-96c6-ac488f6f4980/3193422.pdf
Vancouver
Frota CM, Garib DG, Pinheiro FH de SL, Sathler RC. Self-perception of dentofacial esthetics in individuals with cleft lip and palate [Internet]. Anais. 2019 ;[citado 2024 jun. 02 ] Available from: https://repositorio.usp.br/directbitstream/3a830143-a19c-4b97-96c6-ac488f6f4980/3193422.pdf
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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1038/ejhg.2014.132
Artigo de periodico
Newly recognized autosomal recessive MCA/MR/overgrowth syndrome (1993)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine; Cohen Junior, M. Michael
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e GUION-ALMEIDA, Maria Leine e COHEN JUNIOR, M. Michael. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics, v. 47, n. 2, p. 278-280, 1993Tradução . . Acesso em: 02 jun. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., & Cohen Junior, M. M. (1993). Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics, 47( 2), 278-280.
NLM
Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics. 1993 ; 47( 2): 278-280.[citado 2024 jun. 02 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics. 1993 ; 47( 2): 278-280.[citado 2024 jun. 02 ]
Artigo de periodico
Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents (1993)
Richieri-Costa, Antonio; Pirolo Junior, L; Cohen Junior, M. Michael
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e PIROLO JUNIOR, L e COHEN JUNIOR, M. Michael. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents. American Journal of Medical Genetics, v. 47, n. 2, p. 281-283, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470228. Acesso em: 02 jun. 2024.
APA
Richieri-Costa, A., Pirolo Junior, L., & Cohen Junior, M. M. (1993). Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents. American Journal of Medical Genetics, 47( 2), 281-283. doi:10.1002/ajmg.1320470228
NLM
Richieri-Costa A, Pirolo Junior L, Cohen Junior MM. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents [Internet]. American Journal of Medical Genetics. 1993 ; 47( 2): 281-283.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1002/ajmg.1320470228
Vancouver
Richieri-Costa A, Pirolo Junior L, Cohen Junior MM. Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents [Internet]. American Journal of Medical Genetics. 1993 ; 47( 2): 281-283.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1002/ajmg.1320470228
Artigo de periodico
Newly recognized blepharofacioskeletal syndrome (1993)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine; Rodini, Elaine Sbroggio de Oliveira; Pereira, S C D; Cohen Junior, M. Michael
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio et al. Newly recognized blepharofacioskeletal syndrome. American Journal of Medical Genetics, v. 46, n. 6, p. 620-622, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460603. Acesso em: 02 jun. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., Rodini, E. S. de O., Pereira, S. C. D., & Cohen Junior, M. M. (1993). Newly recognized blepharofacioskeletal syndrome. American Journal of Medical Genetics, 46( 6), 620-622. doi:10.1002/ajmg.1320460603
NLM
Richieri-Costa A, Guion-Almeida ML, Rodini ES de O, Pereira SCD, Cohen Junior MM. Newly recognized blepharofacioskeletal syndrome [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 620-622.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1002/ajmg.1320460603
Vancouver
Richieri-Costa A, Guion-Almeida ML, Rodini ES de O, Pereira SCD, Cohen Junior MM. Newly recognized blepharofacioskeletal syndrome [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 620-622.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1002/ajmg.1320460603

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Source title

Non normalized affiliation

Countries of institutions of collaboration