Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.

Journal: American Journal of Human Genetics

Published: 2019-08-28

DOI: 10.1016/j.ajhg.2019.08.006

Affiliations: 41

Authors: 52

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Institutions Share
Department of Clinical Genetics, Erasmus MC, Netherlands 0.14
Raphael Recanati Genetic Institute, TAU, Israel 0.06
Gleeson Laboratory for Pediatric Brain Diseases, United States of America (USA) 0.06
Centogene AG, Germany 0.06
IRCCS Istituto Giannina Gaslini, Italy 0.05
Erasmus MC-Sophia, Netherlands 0.04
University Hospital Bologna, UNIBO, Italy 0.04
Department of Cell Biology, Erasmus MC, Netherlands 0.04
Department of Pediatrics, UW, United States of America (USA) 0.03
National Research Institute of Mother and Child (NRIMC), Poland 0.03
UC Division of Developmental Biology, United States of America (USA) 0.03
Telethon Institute of Genetics and Medicine (TIGEM), Italy 0.02
Human Genetics and Genome Research Division, NRC, Egypt 0.02
College of Medicine, QU, Saudi Arabia 0.02
Department of Obstetrics and Gynecology, KFSH&RC, Saudi Arabia 0.02
Department of Genetics, KFSH&RC, Saudi Arabia 0.02
Mossakowski Medical Research Centre, PAS, Poland 0.02
Department of Translational Medicine, UNINA, Italy 0.02
Faculty of Medicine, KAU, Saudi Arabia 0.02
NIH National Eye Institute (NEI), United States of America (USA) 0.02
University Medical Center Utrecht (UMC Utrecht), Netherlands 0.02
Center for Medical Genetics, UA, Belgium 0.02
Department of Medical and Surgical Sciences (DIMEC), UNIBO, Italy 0.02
Erasmus University Medical Center (Erasmus MC), Netherlands 0.02
Proteomics Center, Erasmus MC, Netherlands 0.02
Department of Pediatrics, KSU, Saudi Arabia 0.02
Department of Pediatrics, Prince Sultan Military Medical City, Saudi Arabia 0.02
UOC Genetica Medica, IRCCS Istituto Giannina Gaslini, Italy 0.02
Laboratory of Musculoskeletal Cell Biology, IOR, Italy 0.02
IRCCS Istituto delle Scienze Neurologiche di Bologna (ISNB), Italy 0.01
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, and Maternal and Children's Sciences (DINOGMI), University of Genova, Italy 0.01
Center for Integrative Brain Research, Seattle Children's Research Institute, United States of America (USA) 0.01
UC Department of Pediatrics, United States of America (USA) 0.01
Bellaria Hospital, Italy 0.01
Pediatric Neurology Unit, UZ Brussel, Belgium 0.01
Oregon Health and Science University (OHSU), United States of America (USA) 0.01
Rabin Medical Center (RMC), TAU, Israel 0
Felsenstein Medical Research Center (FMRC), TAU, Israel 0
Sackler Faculty of Medicine, TAU, Israel 0