Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly (1999)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1038/9718
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 1999
- Source:
- Título: Nature Genetics
- ISSN: 1061-4036
- Volume/Número/Paginação/Ano: v. 22, n. 2, p. 196-198, June 1999
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
WALLIS, Deeann E. et al. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics, v. 22, n. 2, p. 196-198, 1999Tradução . . Disponível em: https://doi.org/10.1038/9718. Acesso em: 08 fev. 2026. -
APA
Wallis, D. E., Roessler, E., Hehr, U., Nanni, L., Wiltshire, T., Richieri-Costa, A., et al. (1999). Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics, 22( 2), 196-198. doi:10.1038/9718 -
NLM
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly [Internet]. Nature Genetics. 1999 ; 22( 2): 196-198.[citado 2026 fev. 08 ] Available from: https://doi.org/10.1038/9718 -
Vancouver
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly [Internet]. Nature Genetics. 1999 ; 22( 2): 196-198.[citado 2026 fev. 08 ] Available from: https://doi.org/10.1038/9718 - Noonan syndrome in diverse populations
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Informações sobre o DOI: 10.1038/9718 (Fonte: oaDOI API)
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