Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital Malformations.

Journal: American Journal of Human Genetics

Published: 2019-12-16

DOI: 10.1016/j.ajhg.2019.12.004

Affiliations: 23

Authors: 30

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Institutions Share
NIH National Human Genome Research Institute (NHGRI), United States of America (USA) 0.18
University of Wisconsin-Madison (UW-Madison), United States of America (USA) 0.10
Children's National Health System, United States of America (USA) 0.08
Children's Hospital of Philadelphia (CHOP), United States of America (USA) 0.07
Riley Hospital for Children, IU Health, United States of America (USA) 0.07
Department of Pediatrics, UC San Diego, United States of America (USA) 0.07
Texas Scottish Rite Hospital for Children (TSRHC), United States of America (USA) 0.07
University of Toronto (U of T), Canada 0.05
The George Washington University (GW), United States of America (USA) 0.04
Cincinnati Children's Hospital Medical Center (CCHMC), United States of America (USA) 0.03
Mary Bridge Children's Hospital, United States of America (USA) 0.03
University of Missouri Health System, United States of America (USA) 0.03
Washington University in St. Louis (WUSTL), United States of America (USA) 0.03
University Hospital Duesseldorf (UKD), Germany 0.03
Mount Sinai Hospital (MSH), U of T, Canada 0.03
The Hospital for Sick Children (SickKids), U of T, Canada 0.03
Seattle Children's Hospital, United States of America (USA) 0.02
University of Washington (UW), United States of America (USA) 0.02
TUM-HMGU Institute of Human Genetics (IHG), Germany 0.02
TUM University Hospital Klinikum rechts der Isar (MRI), Germany 0.02

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