Bekheirnia, Mir Reza
Bekheirnia, Nasim
Bainbridge, Matthew N.
Gu, Shen
Coban Akdemir, Zeynep Hande
Gambin, Tomek
Janzen, Nicolette K.
Jhangiani, Shalini N.
Muzny, Donna M.
Michael, Mini
Brewer, Eileen D.
Elenberg, Ewa
Kale, Arundhati S.
Riley, Alyssa A.
Swartz, Sarah J.
Scott, Daryl A.
Yang, Yaping
Srivaths, Poyyapakkam R.
Wenderfer, Scott E.
Bodurtha, Joann
Applegate, Carolyn D.
Velinov, Milen
Myers, Angela
Borovik, Lior
Craigen, William J.
Hanchard, Neil A.
Rosenfeld, Jill A.
Lewis, Richard Alan
Gonzales, Edmond T.
Gibbs, Richard A.
Belmont, John W.
Roth, David R.
Eng, Christine
Braun, Michael C.
Lupski, James R.
Lamb, Dolores J.
This article is maintained by: Elsevier
Article Title: Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2016.131
Content Type: article
Copyright: © 2017, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics