Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.

Journal: American Journal of Human Genetics

Published: 2018-08-02

DOI: 10.1016/j.ajhg.2018.07.001

Affiliations: 28

Authors: 52

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Institutions FC
MRC Institute of Genetics and Molecular Medicine (IGMM), The University of Edinburgh, United Kingdom (UK) 0.12
Dubai Hospital, United Arab Emirates 0.08
UCL Great Ormond Street Institute of Child Health (ICH), United Kingdom (UK) 0.08
Biomedical Research Networking Center on Rare Diseases (CIBERER), Spain 0.06
Graduate School of Medicine, Juntendo University, Japan 0.06
The Hospital for Sick Children (SickKids), U of T, Canada 0.04
Chiba Children's Hospital, Japan 0.04
Cologne Center for Genomics (CCG), UoC, Germany 0.04
GeneDx, United States of America (USA) 0.04
Center for Healthy Aging (CEHA), UCPH, Denmark 0.04
Institute of Human Genetics, University of Göttingen, Germany 0.04
Center for Chromosome Stability (CCS), UCPH, Denmark 0.04
Fullerton Genetics Center, Mission Health, United States of America (USA) 0.04
Viapath Group LLP, United Kingdom (UK) 0.04
Department of Genetics and Microbiology (DGM), UAB, Spain 0.04
Hospital La Paz Institute for Health Research (IdiPAZ), Spain 0.03
Department of Pediatrics, CU, United States of America (USA) 0.02
Department of Genetics, KFSH&RC, Saudi Arabia 0.02
Memorial University of Newfoundland (MUN), Canada 0.02
Department of Medical Genetics, KFSH&RC, Saudi Arabia 0.02
Institute for Genomic Medicine (IGM), CU, United States of America (USA) 0.02
Faculty of Medicine, SMU, Japan 0.02
School of Medicine, Marmara University, Turkey 0.02
Instituto de Investigación Hospital 12 de Octubre (i+12), Spain 0.02
School of Medical Education, Newcastle University, United Kingdom (UK) 0.01
Wellcome Trust Centre for Mitochondrial Research, Newcastle University, United Kingdom (UK) 0.01
Institute of Neuroscience (ION), Newcastle University, United Kingdom (UK) 0.01
Institute of Biomedical Research (IIB Sant Pau), Spain 0.01

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