Whole exome sequencing reveals copy number variants in individuals with disorders of sex development

Autor: Sreenivasan, Rajini, Bell, Katrina, van den Bergen, Jocelyn, Robevska, Gorjana, Belluoccio, Daniele, Dahiya, Rachana, Leong, Gary M., Dulon, Jérôme, Touraine, Philippe, Tucker, Elena J., Ayers, Katie, Sinclair, Andrew
Zdroj: In Molecular and Cellular Endocrinology 15 April 2022 546
Databáze: ScienceDirect