Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies (2012)
- Authors:
- USP affiliated authors: ALMEIDA, MARIA LEINE GUION DE - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.a.35305
- Subjects: ANORMALIDADES CRANIOFACIAIS; SÍNDROMES OROFACIODIGITAIS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics, Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 158A, n. 5, p. 1233-1235, May 2012
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RIBEIRO-BICUDO, Lucilene Arilho et al. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies. American Journal of Medical Genetics, Part A, v. 158A, n. 5, p. 1233-1235, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35305. Acesso em: 19 abr. 2024. -
APA
Ribeiro-Bicudo, L. A., Quiezi, R. G., Guion-Almeida, M. L., Legnaro, C., & Richieri-Costa, A. (2012). Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies. American Journal of Medical Genetics, Part A, 158A( 5), 1233-1235. doi:10.1002/ajmg.a.35305 -
NLM
Ribeiro-Bicudo LA, Quiezi RG, Guion-Almeida ML, Legnaro C, Richieri-Costa A. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies [Internet]. American Journal of Medical Genetics, Part A. 2012 ; 158A( 5): 1233-1235.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.35305 -
Vancouver
Ribeiro-Bicudo LA, Quiezi RG, Guion-Almeida ML, Legnaro C, Richieri-Costa A. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies [Internet]. American Journal of Medical Genetics, Part A. 2012 ; 158A( 5): 1233-1235.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.35305 - Disostose fronto-nasal: aspectos clínicos e genéticos
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Informações sobre o DOI: 10.1002/ajmg.a.35305 (Fonte: oaDOI API)
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