Source: Journal of molecular diagnostics. Unidade: FM
Subjects: CONHECIMENTO, FENÓTIPOS, PACIENTES, GENES, DOENÇAS
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: 17 out. 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.2020.05.007NLM
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 out. 17 ] Available from: https://doi.org/10.1016/j.jmoldx.2020.05.007Vancouver
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 out. 17 ] Available from: https://doi.org/10.1016/j.jmoldx.2020.05.007