De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies.

Journal: American Journal of Human Genetics

Published: 2019-07-23

DOI: 10.1016/j.ajhg.2019.07.005

Affiliations: 28

Authors: 34

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Institutions Share
Faculty of Health and Life Sciences, Brookes, United Kingdom (UK) 0.10
IRCCS Bambino Gesù Children's Hospital, Italy 0.09
West Midlands Regional Genetics Laboratory, Birmingham Women's and Children's NHS Foundation Trust, United Kingdom (UK) 0.09
Duke Department of Pediatrics, United States of America (USA) 0.07
Department of Clinical Genetics, OUH SDU, Denmark 0.06
Neurology and Neurogenetics Clinic, Kennedy Krieger Institute, United States of America (USA) 0.06
UCL Great Ormond Street Institute of Child Health (ICH), United Kingdom (UK) 0.06
UMC Section Genetics, Netherlands 0.06
Epidermis Differentiation and Rheumatoid Autoimmunity (UDEAR), France 0.06
UCL Research Department of Cell and Developmental Biology (CDB), United Kingdom (UK) 0.04
UCSF School of Medicine, United States of America (USA) 0.03
Hôpital Purpan, CHU-Toulouse, France 0.03
Ambry Genetics, United States of America (USA) 0.03
Odense University Hospital (OUH), Denmark 0.03
IRCCS Casa Sollievo della Sofferenza Hospital, Italy 0.03
IRCCS Oasi Maria Santissima, Italy 0.03
Duke Department of Neurobiology, United States of America (USA) 0.01
AstraZeneca Cambridge, United Kingdom (UK) 0.01
University of Washington (UW), United States of America (USA) 0.01
Department of Medicine and Radiology, UniMelb, Australia 0.01
UCL Institute of Ophthalmology (IoO), United Kingdom (UK) 0.01
Center for Integrative Brain Research, Seattle Children's Research Institute, United States of America (USA) 0.01
Faculty of Medicine, CU, Egypt 0.01
The Mindich Child Health and Development Institute (MCHDI), ISMMS, United States of America (USA) 0.01
Department of Pediatrics, ISMMS, United States of America (USA) 0.01
Department of Genetics and Genomic Sciences, ISMMS, United States of America (USA) 0.01

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