Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil (2024)
- Authors:
- USP affiliated authors: CARVALHO, WERTHER BRUNOW DE - FM ; KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1002/ajmg.a.63544
- Subjects: SEQUENCIAMENTO GENÉTICO; DIAGNÓSTICO; CRIANÇAS; BRASIL
- Language: Inglês
- Imprenta:
- Source:
- Título: American journal of medical genetics part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 194, n. 6, 2024
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
MIGLIAVACCA, Michele P et al. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil. American journal of medical genetics part A, v. 194, n. 6, 2024Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/77006. Acesso em: 08 jun. 2025. -
APA
Migliavacca, M. P., Sobreira, J., Bermeo, D., Gomes, M., Alencar, D., Sussuchi, L., et al. (2024). Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil. American journal of medical genetics part A, 194( 6). doi:10.1002/ajmg.a.63544 -
NLM
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Carvalho WB de, Kim CA. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil [Internet]. American journal of medical genetics part A. 2024 ; 194( 6):[citado 2025 jun. 08 ] Available from: https://observatorio.fm.usp.br/handle/OPI/77006 -
Vancouver
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Carvalho WB de, Kim CA. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil [Internet]. American journal of medical genetics part A. 2024 ; 194( 6):[citado 2025 jun. 08 ] Available from: https://observatorio.fm.usp.br/handle/OPI/77006 - Contribuicao para o estudo da osteogenese imperfeita: aspectos genetico-clinicos de 25 casos
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Informações sobre o DOI: 10.1002/ajmg.a.63544 (Fonte: oaDOI API)
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