Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? (2009)
- Authors:
- USP affiliated authors: COSTA, ANTONIO RICHIERI DA - HRAC ; OTTO, PAULO ALBERTO - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: HRAC; IB
- DOI: 10.1002/ajmg.a.32849
- Subjects: MALFORMAÇÕES; LÁBIO FISSURADO; PALATO
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics. Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 149A, n. 6, p. 1319-1322, 2009
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
JEHEE, Fernanda Sarquis et al. Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done?. American Journal of Medical Genetics. Part A, v. 149A, n. 6, p. 1319-1322, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32849. Acesso em: 13 fev. 2026. -
APA
Jehee, F. S., Burin, B. A., Rocha, K. M. da, Zechi-Ceide, R. M., Bueno, D. F., Brito, L., et al. (2009). Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? American Journal of Medical Genetics. Part A, 149A( 6), 1319-1322. doi:10.1002/ajmg.a.32849 -
NLM
Jehee FS, Burin BA, Rocha KM da, Zechi-Ceide RM, Bueno DF, Brito L, Souza J, Leal GF, Richieri-Costa A, Alonso N, Otto PA, Passos-Bueno MR. Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1319-1322.[citado 2026 fev. 13 ] Available from: https://doi.org/10.1002/ajmg.a.32849 -
Vancouver
Jehee FS, Burin BA, Rocha KM da, Zechi-Ceide RM, Bueno DF, Brito L, Souza J, Leal GF, Richieri-Costa A, Alonso N, Otto PA, Passos-Bueno MR. Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1319-1322.[citado 2026 fev. 13 ] Available from: https://doi.org/10.1002/ajmg.a.32849 - Screening of c934g and c937g mutations among patients with craniosynostosis reveals two apert patients not caused by any of these mutations
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Informações sobre o DOI: 10.1002/ajmg.a.32849 (Fonte: oaDOI API)
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