Source: Genetics and Molecular Biology. Unidade: IB
Subjects: MALFORMAÇÕES (CONGÊNITO), DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
ABNT
ALVES, Leandro Ucela et al. A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome. Genetics and Molecular Biology, v. 38, n. 1, p. 37-41, 2015Tradução . . Disponível em: https://doi.org/10.1590/S1415-475738120140125. Acesso em: 06 jul. 2024.APA
Alves, L. U., Pardono, E., Otto, P. A., & Mingroni Netto, R. C. (2015). A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome. Genetics and Molecular Biology, 38( 1), 37-41. doi:10.1590/S1415-475738120140125NLM
Alves LU, Pardono E, Otto PA, Mingroni Netto RC. A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome [Internet]. Genetics and Molecular Biology. 2015 ; 38( 1): 37-41.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1590/S1415-475738120140125Vancouver
Alves LU, Pardono E, Otto PA, Mingroni Netto RC. A novel c.1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome [Internet]. Genetics and Molecular Biology. 2015 ; 38( 1): 37-41.[citado 2024 jul. 06 ] Available from: https://doi.org/10.1590/S1415-475738120140125