Ribeiro-Bicudo, Lucilene Arilho 
; Quiezi, Rodrigo Gonçalves; Guion-Almeida, Maria Leine; Legnaro, Chiara; Richieri-Costa, Antonio
Fonte: American Journal of Medical Genetics, Part A. Unidade: HRAC
Assuntos: ANORMALIDADES CRANIOFACIAIS, SÍNDROMES OROFACIODIGITAIS
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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: 05 out. 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.35305NLM
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 out. 05 ] Available from: https://doi.org/10.1002/ajmg.a.35305Vancouver
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 out. 05 ] Available from: https://doi.org/10.1002/ajmg.a.35305
