Application of whole exome sequencing in detecting copy number variants in patients with developmental delay and/or multiple congenital malformations

Publication date: Available online 1 June 2020Source: The Journal of Molecular DiagnosticsAuthor(s): Évelin A. Zanardo, Fabíola P. Monteiro, Samar N. Chehimi, Yanca G. Oliveira, Alexandre T. Dias, Larissa A. Costa, Luiza L. Ramos, Gil M. Novo-Filho, Marília M. Montenegro, Amom M. Nascimento, João P. Kitajima, Fernando Kok, Leslie D. Kulikowski
Source: The Journal of Molecular Diagnostics - Category: Pathology Source Type: research