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Kidney International|March 1, 2022
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tractJohannes Münch, Marie Engesser, Ria Schönauer, et al.HGG Advances|December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart diseasePolakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.Genome Biology|July 18, 2018
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6Bram P Prins, Timothy J Mead, Jennifer A Brody, et al.Pageof 43