Clinical application of whole-exome sequencing across clinical indications

作者：Kyle Retterer, Jane Juusola, Megan T. Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G. Monaghan, Dianalee McKnight, Renkui Bai, Sharon F. Suchy, Bethany Friedman, Jackie Tahiliani, Daniel Pineda‐Alvarez, Gabriele Richard, Tracy Brandt, Eden V. Haverfield, Wendy K. Chung, Sherri J. Bale · 发表于：Genetics in Medicine · 年份：2015 · DOI：10.1038/gim.2015.148 · 被引用次数：1097 · 研究领域：Genomics and Rare Diseases、Genomic variations and chromosomal abnormalities、Connective tissue disorders research