Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.

Autor: Normand, Elizabeth A.1 (AUTHOR) liznormand@gmail.com, Braxton, Alicia1,2 (AUTHOR) acarlson@bcm.edu, Nassef, Salma1 (AUTHOR) salma.nassef@bcm.edu, Ward, Patricia A.1,2 (AUTHOR) pward@bcm.edu, Vetrini, Francesco2 (AUTHOR) vetrini@bcm.edu, He, Weimin2 (AUTHOR) weimin.he@bcm.edu, Patel, Vipulkumar2 (AUTHOR) vipul.patel@bcm.edu, Qu, Chunjing2 (AUTHOR) chunjing.qu@bcm.edu, Westerfield, Lauren E.1 (AUTHOR) lewester@texaschildrens.org, Stover, Samantha1 (AUTHOR) srstover@texaschildrens.org, Dharmadhikari, Avinash V.2 (AUTHOR) avinashd.9@gmail.com, Muzny, Donna M.1,3 (AUTHOR) donnam@bcm.edu, Gibbs, Richard A.1,3 (AUTHOR) agibbs@bcm.edu, Dai, Hongzheng1 (AUTHOR) hongzheng.dai@bcm.edu, Meng, Linyan1,2 (AUTHOR) lmeng@bcm.edu, Wang, Xia1,2 (AUTHOR) xiaw@bcm.edu, Xiao, Rui1,2 (AUTHOR) rx147432@bcm.edu, Liu, Pengfei1,2 (AUTHOR) pengfeil@bcm.edu, Bi, Weimin1,2 (AUTHOR) wbi@bcm.edu, Xia, Fan1,2 (AUTHOR) fxia@bcm.edu
Zdroj: Genome Medicine. 9/28/2018, Vol. 10 Issue 1, p1-14. 14p.
Databáze: Academic Search Ultimate
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