Application of Whole-Exome Sequencing in for updates Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations (2020)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1016/j.jmoldx.2020.05.007
- Subjects: CONHECIMENTO; FENÓTIPOS; PACIENTES; GENES; DOENÇAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of molecular diagnostics
- ISSN: 1525-1578
- Volume/Número/Paginação/Ano: v. 22, n. 8, p. 1041-1049, 2020
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: publisher-specific-oa
-
ABNT
ZANARDO, Evelin A et al. Application of Whole-Exome Sequencing in for updates Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations. Journal of molecular diagnostics, v. 22, n. 8, p. 1041-1049, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jmoldx.2020.05.007. Acesso em: 01 jun. 2024. -
APA
Zanardo, E. A., Monteiro, F. P., Chehimi, S. N., Oliveira, Y. G. de, Dias, A. T., Costa, L. A., et al. (2020). Application of Whole-Exome Sequencing in for updates Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations. Journal of molecular diagnostics, 22( 8), 1041-1049. doi:10.1016/j.jmoldx.2020.05.007 -
NLM
Zanardo EA, Monteiro FP, Chehimi SN, Oliveira YG de, Dias AT, Costa LA, Ramos LL, Novo-Filho GM, Montenegro MM, Kok F. Application of Whole-Exome Sequencing in for updates Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations [Internet]. Journal of molecular diagnostics. 2020 ; 22( 8): 1041-1049.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.jmoldx.2020.05.007 -
Vancouver
Zanardo EA, Monteiro FP, Chehimi SN, Oliveira YG de, Dias AT, Costa LA, Ramos LL, Novo-Filho GM, Montenegro MM, Kok F. Application of Whole-Exome Sequencing in for updates Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations [Internet]. Journal of molecular diagnostics. 2020 ; 22( 8): 1041-1049.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.jmoldx.2020.05.007 - Encefalopatias progressivas em crianças
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Informações sobre o DOI: 10.1016/j.jmoldx.2020.05.007 (Fonte: oaDOI API)
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