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Haggerty, Kelsey
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BEKHEIRNIA, MIR REZA
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Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+).
Academic Article
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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
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Multidisciplinary K12 Urologic Research Career Development Program; M. R. Bekheirnia was a K12 scholar
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Improving the Diagnosis of Congenital Genitourinary Birth Defects
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SCOTT, DARYL
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POSEY, JENNIFER
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LUNA, PAMELA
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SHAW, CHAD
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LUPSKI, JAMES
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PEHLIVAN, DAVUT
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