Publications

Export 1 results:
Author Title [ Year(Desc)]
Filters: Author is Swartz, Sarah J  [Clear All Filters]
2017
Bekheirnia, M. Reza et al. 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. Genet Med 19, 412-420 (2017).