Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Lee H, Deignan JL, Dorrani N, Strom SP, Kantarci S, Quintero-Rivera F, Das K, Toy T, Harry B, Yourshaw M, Fox M, Fogel BL, Martinez-Agosto JA, Wong DA, Chang VY, Shieh PB, Palmer CG, Dipple KM, Grody WW, Vilain E, Nelson SF.
Lee H, et al. Among authors: chang vy.
JAMA. 2014 Nov 12;312(18):1880-7. doi: 10.1001/jama.2014.14604.
JAMA. 2014.
PMID: 25326637
Free PMC article.