Clinical Report of a 17q12 Microdeletion with Additionally Unreported Clinical Features

por Roberts, Jennifer L., Gandomi, Stephanie K., Parra, Melissa, Lu, Ira, Gau, Chia-Ling, Dasouki, Majed, Butler, Merlin G.
Publicado 2014

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients

por LaDuca, Holly, Stuenkel, A J, Dolinsky, Jill S., Keiles, Steven, Tandy, Stephany, Pesaran, Tina, Chen, Elaine, Gau, Chia-Ling, Palmaer, Erika, Shoaepour, Kamelia, Shah, Divya, Speare, Virginia, Gandomi, Stephanie, Chao, Elizabeth
Publicado 2014