Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort (2012)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/bdra.23047
- Subjects: HOLOPROSENCEFALIA; POLIMORFISMO; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Birth Defects Research. Part A, Clinical and Molecular Teratology.
- ISSN: 1542-0752
- Volume/Número/Paginação/Ano: v. 94, n. 11, p. 912-917, Nov. 2012
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
RIBEIRO, Lucilene Arilho et al. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort. Birth Defects Research. Part A, Clinical and Molecular Teratology., v. No 2012, n. 11, p. 912-917, 2012Tradução . . Disponível em: https://doi.org/10.1002/bdra.23047. Acesso em: 24 fev. 2026. -
APA
Ribeiro, L. A., Roessler, E., Hu, P., Pineda-Alvarez, D. E., Zhou, N., Jones, M. P., et al. (2012). Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort. Birth Defects Research. Part A, Clinical and Molecular Teratology., No 2012( 11), 912-917. doi:10.1002/bdra.23047 -
NLM
Ribeiro LA, Roessler E, Hu P, Pineda-Alvarez DE, Zhou N, Jones MP, Chandrasekharappa S, Richieri-Costa A, Muenke M. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort [Internet]. Birth Defects Research. Part A, Clinical and Molecular Teratology. 2012 ; No 2012( 11): 912-917.[citado 2026 fev. 24 ] Available from: https://doi.org/10.1002/bdra.23047 -
Vancouver
Ribeiro LA, Roessler E, Hu P, Pineda-Alvarez DE, Zhou N, Jones MP, Chandrasekharappa S, Richieri-Costa A, Muenke M. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort [Internet]. Birth Defects Research. Part A, Clinical and Molecular Teratology. 2012 ; No 2012( 11): 912-917.[citado 2026 fev. 24 ] Available from: https://doi.org/10.1002/bdra.23047 - Noonan syndrome in diverse populations
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Informações sobre o DOI: 10.1002/bdra.23047 (Fonte: oaDOI API)
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