Pleiotropy of Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Phenotypes in Human 16p11.2 Microdeletion Syndrome Is Recapitulated in Mouse Models of Tbx6 Deletion
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S. Bauer | Shrikant Mane | V. Tasic | F. Hildebrandt | Steve Seltzsam | Chunyan Wang | B. Zheng | Nina Mann | D. Connaughton | Sophia R Schneider | L. Schierbaum | M. Nakayama | R. Dai | N. Stajić | Jeremiah Martino | S. Shril | C. Wu | Simone Sanna-Cherchi | Hyun Joo Nam | Gregory B. Whittemore | Dervla M. Connaughton | Yask Gupta | Cathy L. Mendelsohn | T. Y. Lim