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 NHGRI Medical Genetics Branch, United States of America (USA) 0.18
Riley Hospital for Children, IU Health, United States of America (USA) 0.07
Division of Human Genetics, CHOP, United States of America (USA) 0.07
Texas Scottish Rite Hospital for Children (TSRHC), United States of America (USA) 0.07
Department of Pediatrics, UC San Diego, United States of America (USA) 0.07
Molecular and Environmental Toxicology Center (METC), UW-Madison, United States of America (USA) 0.05
Department of Comparative Biosciences, UW-Madison, United States of America (USA) 0.05
Center for Genetic Medicine Research, Children's National Health System, United States of America (USA) 0.04
Department of Genomics and Precision Medicine, GW, United States of America (USA) 0.04
Division of Genetics and Genomic Medicine, WUSTL, United States of America (USA) 0.03
School of Medicine, Mizzou, United States of America (USA) 0.03
Department of Endocrinology and Diabetology, HHU, Germany 0.03
UC Division of Endocrinology, United States of America (USA) 0.03
Children's Research Institute (CRI), Children's National Health System, United States of America (USA) 0.03
Mary Bridge Children's Hospital, United States of America (USA) 0.03
Division of Clinical and Metabolic Genetics, SickKids U of T, Canada 0.03
Mount Sinai Hospital (MSH), U of T, Canada 0.03
Department of Obstetrics and Gynaecology, U of T, Canada 0.03
Department of Paediatrics, U of T, Canada 0.03
TUM-HMGU Institute of Human Genetics (IHG), Germany 0.02
University of Washington (UW), United States of America (USA) 0.02
Seattle Children's Hospital, United States of America (USA) 0.02
TUM University Hospital Klinikum rechts der Isar (MRI), Germany 0.02

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