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22. Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT

30. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

32. A Genetic Map of the Response to DNA Damage in Human Cells

36. A Human Depression Circuit Derived From Focal Brain Lesions

43. Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

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