EDA mutation by exome sequencing in non-syndromic X-linked oligodontia (2017)
Source: Clinical Genetics. Unidade: ESALQ
Subjects: ANOMALIA DENTÁRIA, MAPEAMENTO GENÉTICO, MUTAÇÃO GENÉTICA
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MARTINS, L et al. EDA mutation by exome sequencing in non-syndromic X-linked oligodontia. Clinical Genetics, v. 92, n. 2, p. 227-229, 2017Tradução . . Disponível em: https://doi.org/10.1111/cge.12961. Acesso em: 18 out. 2024.APA
Martins, L., Machado, R. A., Araujo, D. S., Giovani, P. A., Rebouças, P. D., Rodrigues, L. P., et al. (2017). EDA mutation by exome sequencing in non-syndromic X-linked oligodontia. Clinical Genetics, 92( 2), 227-229. doi:10.1111/cge.12961NLM
Martins L, Machado RA, Araujo DS, Giovani PA, Rebouças PD, Rodrigues LP, Mofatto LS, Ribeiro MM, Coutinho LL, Puppin-Rontani RM, Coletta RD, Nociti Junior FH, Kantovitz KR. EDA mutation by exome sequencing in non-syndromic X-linked oligodontia [Internet]. Clinical Genetics. 2017 ; 92( 2): 227-229.[citado 2024 out. 18 ] Available from: https://doi.org/10.1111/cge.12961Vancouver
Martins L, Machado RA, Araujo DS, Giovani PA, Rebouças PD, Rodrigues LP, Mofatto LS, Ribeiro MM, Coutinho LL, Puppin-Rontani RM, Coletta RD, Nociti Junior FH, Kantovitz KR. EDA mutation by exome sequencing in non-syndromic X-linked oligodontia [Internet]. Clinical Genetics. 2017 ; 92( 2): 227-229.[citado 2024 out. 18 ] Available from: https://doi.org/10.1111/cge.12961