Fonte: American journal of medical genetics. Unidade: FM
Assuntos: CARDIOPATIAS CONGÊNITAS, DELEÇÃO DE GENES, ESTUDOS DE COORTES
ABNT
ZAMARIOLLI, Malu et al. Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort. American journal of medical genetics, v. 191, n. 5, p. 1273-1281, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/53995. Acesso em: 20 out. 2024.APA
Zamariolli, M., Dantas, A. G., Nunes, N., Moyses-Oliveira, M., Sgardioli, I. C., Soares, D. C. de Q., et al. (2023). Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort. American journal of medical genetics, 191( 5), 1273-1281. doi:10.1002/ajmg.a.63145NLM
Zamariolli M, Dantas AG, Nunes N, Moyses-Oliveira M, Sgardioli IC, Soares DC de Q, Gil-da-Silva-Lopes VL, Kim CA, Melaragno MI de SA. Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort [Internet]. American journal of medical genetics. 2023 ; 191( 5): 1273-1281.[citado 2024 out. 20 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53995Vancouver
Zamariolli M, Dantas AG, Nunes N, Moyses-Oliveira M, Sgardioli IC, Soares DC de Q, Gil-da-Silva-Lopes VL, Kim CA, Melaragno MI de SA. Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort [Internet]. American journal of medical genetics. 2023 ; 191( 5): 1273-1281.[citado 2024 out. 20 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53995