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Match	Type	Why
BEKHEIRNIA, MIR REZA	Person	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 scholar	Grant	Why?
Improving the Diagnosis of Congenital Genitourinary Birth Defects	Grant	Why?
LUPSKI, JAMES	Person	Why?
PEHLIVAN, DAVUT	Person	Why?
POSEY, JENNIFER	Person	Why?

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