Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss.

Sheppard, Sarah; Biswas, Sawona; Li, Mindy H; Jayaraman, Vijayakumar; Slack, Ian; Romasko, Edward J; Sasson, Ariella; Brunton, Joshua; Rajagopalan, Ramakrishnan; Sarmady, Mahdi; Abrudan, Jenica L; Jairam, Sowmya; DeChene, Elizabeth T; Ying, Xiahoan; Choi, Jiwon; Wilkens, Alisha; Raible, Sarah E; Scarano, Maria I; Santani, Avni; Pennington, Jeffrey W; Luo, Minjie; Conlin, Laura K; Devkota, Batsal; Dulik, Matthew C; Spinner, Nancy B; Krantz, Ian D.
Genet Med; 20(12): 1663-1676, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-29907799