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
Open Access
- 1 April 2017
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 19 (4), 412-420
- https://doi.org/10.1038/gim.2016.131
Abstract
No abstract availableKeywords
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