Bi-allelic TMEM94 Truncating Variants Are Associated with Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial Dysmorphism.

Journal: American Journal of Human Genetics

Published: 2018-12-06

DOI: 10.1016/j.ajhg.2018.11.001

Affiliations: 22

Authors: 38

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Institutions FC
NIH NHGRI Human Biochemical Genetics Section, United States of America (USA) 0.12
UCLA Department of Human Genetics, United States of America (USA) 0.12
Department of Genetics, KFSH&RC, Saudi Arabia 0.09
Department of Pediatrics, HMC, Qatar 0.08
NIH National Human Genome Research Institute (NHGRI), United States of America (USA) 0.07
NIH NHGRI Undiagnosed Diseases Network (UDN), United States of America (USA) 0.07
NIH National Institute of Dental and Craniofacial Research (NIDCR), United States of America (USA) 0.05
Department of Medical Genetics, MAHE, India 0.05
Clinical Research Priority Program (CRPP) / Rare Disease Initiative Zurich (RADIZ), UZH, Switzerland 0.04
UCLA Department of Pathology and Laboratory Medicine, United States of America (USA) 0.04
Institute of Medical Genetics (IMG), UZH, Switzerland 0.04
Mazumdar Shaw Medical Center, NH, India 0.03
NIH Division of Veterinary Resources (DVR), United States of America (USA) 0.03
University Children's Hospital of Zurich, Switzerland 0.03
Narayana Institute of Cardiac Sciences, NH, India 0.03
NIH NHGRI Cancer Genetics and Comparative Genomics Branch, United States of America (USA) 0.03
Department of Pediatric Genetics, Amrita University, India 0.03
Biostatistics Epidemiology & Scientific Computing (BESC), KFSH&RC, Saudi Arabia 0.03
NIH National Institute of Neurological Disorders and Stroke (NINDS), United States of America (USA) 0.03
Saudi Human Genome Program, KACST, Saudi Arabia 0.01
Department of Anatomy and Cell Biology, Alfaisal University, Saudi Arabia 0.01

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