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Application of whole exome sequencing in detecting copy number variants in patients with developmental delay and/or multiple congenital malformations
Zanardo, Ãvelin A., Monteiro, FabÃola P., Chehimi, Samar N., Oliveira, Yanca G., Dias, Alexandre T., Costa, Larissa A., Ramos, Luiza L., Novo-Filho, Gil M., Montenegro, MarÃlia M., Nascimento, AmomJournal:
The Journal of Molecular Diagnostics
DOI:
10.1016/j.jmoldx.2020.05.007
Date:
June, 2020
File:
PDF, 527 KB
2020