학술논문
Genomic sequencing identifies secondary findings in a cohort of parent study participants
Document Type
Article
Author
Thompson, Michelle L.; Finnila, Candice R.; Bowling, Kevin M.; Brothers, Kyle B.; Neu, Matthew B.; Amaral, Michelle D.; Hiatt, Susan M.; East, Kelly M.; Gray, David E.; Lawlor, James M.J.; Kelley, Whitley V.; Lose, Edward J.; Rich, Carla A.; Simmons, Shirley; Levy, Shawn E.; Myers, Richard M.; Barsh, Gregory S.; Bebin, E Martina; Cooper, Gregory M.
Source
Genetics in Medicine; December 2018, Vol. 20 Issue: 12 p1635-1643, 9p
Subject
Language
ISSN
10983600; 15300366
Abstract
Clinically relevant secondary variants were identified in parents enrolled with a child with developmental delay and intellectual disability.