KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis

Journal: American Journal of Human Genetics

Published: 2018-01-04

DOI: 10.1016/j.ajhg.2017.12.002

Affiliations: 34

Authors: 39

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Institutions FC
Center for Integrative Genomics (CIG), UNIL, Switzerland 0.13
Faculty of Medicine, VU, Lithuania 0.10
Swiss Institute of Bioinformatics (SIB), Switzerland 0.10
UMC Department of Medical Genetics, Netherlands 0.08
Department of Genetics, KFSH&RC, Saudi Arabia 0.06
KK Women's and Children's Hospital (KKH), Singapore 0.05
Hospices Civils de Lyon (HCL), France 0.05
Department of Obstetrics and Gynecology, KFSH&RC, Saudi Arabia 0.05
Department of Genetic Medicine and Development, UNIGE, Switzerland 0.05
Lyon Neuroscience Research Center (CRNL), France 0.04
Institute of Medical Biology (IMB), A*STAR, Singapore 0.03
Institute of Genetics and Molecular and Cellular Biology (IGBMC), France 0.03
Center for Fetal Research, CHOP, United States of America (USA) 0.03
Claude Bernard University Lyon 1 (UCBL), France 0.03
University Hospitals of Strasbourg (HUS), France 0.03
University Hospital Bologna, UNIBO, Italy 0.03
Wellcome Trust Genome Campus, United Kingdom (UK) 0.03
Royal Devon and Exeter NHS Foundation Trust, United Kingdom (UK) 0.03
Hôpital Femme Mère Enfant (HFME), HCL, France 0.01
Duke-NUS Graduate Medical School Singapore, Singapore 0.01
Lee Kong Chian School of Medicine, Singapore 0.01
Department of Anatomy and Cell Biology, Alfaisal University, Saudi Arabia 0.01
Saudi Human Genome Program, KACST, Saudi Arabia 0.01
Institute of Molecular and Cell Biology (IMCB), A*STAR, Singapore 0.01
NUS Department of Paediatrics, Singapore 0.01
Amsterdam Reproduction and Development, Netherlands 0.01

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