Search Results (11)

MatchTypeWhy
BEKHEIRNIA, MIR REZAPerson Why?
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+).Academic Article Why?
Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome.Academic Article Why?
Multidisciplinary K12 Urologic Research Career Development Program; M. R. Bekheirnia was a K12 scholarGrant Why?
Improving the Diagnosis of Congenital Genitourinary Birth DefectsGrant Why?
SCOTT, DARYLPerson Why?
POSEY, JENNIFERPerson Why?
LUNA, PAMELAPerson Why?
SHAW, CHADPerson Why?
LUPSKI, JAMESPerson Why?
PEHLIVAN, DAVUTPerson Why?
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