Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848

Journal: American Journal of Human Genetics

Published: 2018-01-04

DOI: 10.1016/j.ajhg.2017.12.001

Affiliations: 54

Authors: 75

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Institutions FC
UAB Department of Genetics, United States of America (USA) 0.15
Children's Hospitals and Clinics of Minnesota, United States of America (USA) 0.04
Centre de Génétique Humaine, IPG, Belgium 0.04
Dell Children’s Medical Center, Seton Healthcare Family, United States of America (USA) 0.03
SA Pathology, Australia 0.03
Johns Hopkins All Children’s Hospital, United States of America (USA) 0.03
Genomic Medicine Institute (GMI), Cleveland Clinic, United States of America (USA) 0.03
Division of Genetics and Metabolism, Children's National Health System, United States of America (USA) 0.03
Health Innovation Manchester, United Kingdom (UK) 0.03
Center for Medical Genetics (CMGG), UGent, Belgium 0.03
Children's Hospital of Michigan, DMC, United States of America (USA) 0.03
Department of Medical Genetics, McGill University, Canada 0.03
Children's Hospital of Philadelphia (CHOP), United States of America (USA) 0.02
Perelman School of Medicine, Penn, United States of America (USA) 0.02
Mayo Clinic's Campus in Arizona, United States of America (USA) 0.01
IRCCS Carlo Besta Neurological Institute, Italy 0.01
Birmingham Women's and Children's NHS Foundation Trust, United Kingdom (UK) 0.01
NYU Department of Pediatrics, United States of America (USA) 0.01
Department of Neurology, MGH, United States of America (USA) 0.01
Cancer Center, MGH, United States of America (USA) 0.01
Faculty of Medicine (FMUSP), USP, Brazil 0.01
Univeristy of Minnesota Health, United States of America (USA) 0.01
Tel Aviv Sourasky Medical Center, Israel 0.01
Boston Children's Hospital (BCH), United States of America (USA) 0.01
Department of Neurology, BCH, United States of America (USA) 0.01
Institute of Cancer and Genetics, Cardiff University, United Kingdom (UK) 0.01
Department of Clinical Genetics, Erasmus MC, Netherlands 0.01
Department of Pediatrics, UGent, Belgium 0.01
Department of Molecular Genetics and Microbiology (MGM), UF, United States of America (USA) 0.01
OHSU Department of Molecular and Medical Genetics (MMG), United States of America (USA) 0.01
IRCCS Molecular Neuro-Oncology Unit, Italy 0.01
Center for Medical Genetics, UA, Belgium 0.01
Department of Neurology and Neurosurgery, JHU, United States of America (USA) 0.01
Biomedical Research Networking Center on Rare Diseases (CIBERER), Spain 0.01
Stony Brook Children's, SUNY Stony Brook, United States of America (USA) 0.01
IRCCS Casa Sollievo della Sofferenza Hospital, Italy 0.01
Nemours/Alfred I. duPont Hospital for Children, United States of America (USA) 0.01
Department of Molecular and Human Genetics, BCM, United States of America (USA) 0.01
St George's University Hospitals NHS Foundation Trust, United Kingdom (UK) 0.01
Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Spain 0.01
Department of Human Genetics, KU Leuven, Belgium 0.01
Faculdade de Medicina (CMM), UFF, Brazil 0.01
Children's Hospital at Westmead (CHW), USYD, Australia 0.01
Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, United Kingdom (UK) 0.01
Sheffield Clinical Genetics Department, Sheffield Children's NHS Foundation Trust, United Kingdom (UK) 0.01
Valley Children's Healthcare, United States of America (USA) 0.01
Miami Cancer Institute, United States of America (USA) 0.01
Yale Department of Genetics, United States of America (USA) 0.01
Istituto di Ricerca Pediatrica Città della Speranza (IRP), Italy 0.01
Universidad de Oriente (UDO), Venezuela 0.01
Felipe Guevara Rojas Hospital, Venezuela 0.01
Division of Medical Sciences, NCCS, Singapore 0.01
Adelaide Medical School, Adelaide Uni, Australia 0.01
Department of Women's and Children's Health (SDB), UNIPD, Italy 0.01

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