De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic Features.

Journal: American Journal of Human Genetics

Published: 2018-07-05

DOI: 10.1016/j.ajhg.2018.06.005

Affiliations: 17

Authors: 36

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Institutions FC
Department of Molecular and Human Genetics, BCM, United States of America (USA) 0.31
Baylor Genetics, United States of America (USA) 0.17
NIH NHGRI Undiagnosed Diseases Network (UDN), United States of America (USA) 0.14
Stanford School of Medicine, United States of America (USA) 0.07
Texas Children's Hospital, BCM, United States of America (USA) 0.07
Stanford Lucile Packard Children's Hospital (LPCH), United States of America (USA) 0.04
University of Alabama at Birmingham (UAB), United States of America (USA) 0.03
UCSF Prenatal Diagnostic Center, United States of America (USA) 0.03
NIH National Human Genome Research Institute (NHGRI), United States of America (USA) 0.03
Department of Obstetrics and Gynaecology, U of T, Canada 0.03
Prenatal Diagnosis and Medical Genetics, U of T, Canada 0.03
Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital (NRI), United States of America (USA) 0.02
Le Bonheur Children's Hospital, UTHSC, United States of America (USA) 0.01
University of Tennessee Health Science Center (UTHSC), United States of America (USA) 0.01
Institute for Genetics, UoC, Germany 0.01
Center for Molecular Medicine Cologne (CMMC), UoC, Germany 0.01
Center for Rare Diseases Cologne (ZSEK), UoC, Germany 0.01

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