PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI (2006)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.a.31369
- Subjects: FISSURA LÁBIOPALATINA; ANORMALIDADES MÚLTIPLAS; HOLOPROSENCEFALIA; MUTAÇÃO; FENÓTIPOS
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 140A, n. 23, p. 2584-2586, Dec. 2006
- Status:
- Nenhuma versão em acesso aberto identificada
-
ABNT
RIBEIRO, Lucilene Arilho e MURRAY, Jeffrey C. e RICHIERI-COSTA, Antonio. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI. American Journal of Medical Genetics Part A, v. 140A, n. 23, p. 2584-2586, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31369. Acesso em: 18 mar. 2026. -
APA
Ribeiro, L. A., Murray, J. C., & Richieri-Costa, A. (2006). PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI. American Journal of Medical Genetics Part A, 140A( 23), 2584-2586. doi:10.1002/ajmg.a.31369 -
NLM
Ribeiro LA, Murray JC, Richieri-Costa A. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2584-2586.[citado 2026 mar. 18 ] Available from: https://doi.org/10.1002/ajmg.a.31369 -
Vancouver
Ribeiro LA, Murray JC, Richieri-Costa A. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2584-2586.[citado 2026 mar. 18 ] Available from: https://doi.org/10.1002/ajmg.a.31369 - Noonan syndrome in diverse populations
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