Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals
Status PubMed-not-MEDLINE Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu tisková chyba
Grantová podpora
F30 HD112125
NICHD NIH HHS - United States
PubMed
39060653
PubMed Central
PMC11292024
DOI
10.1038/s41431-024-01659-y
PII: 10.1038/s41431-024-01659-y
Knihovny.cz E-zdroje
- Publikační typ
- tisková chyba MeSH
Applied and Translational Neurogenomics Group VIB Center for Molecular Neurology Antwerp Belgium
Boston Children's Hospital Boston MA USA
Center of Medical Genetics Antwerp University Hospital University of Antwerp Edegem Belgium
Charles University 1st Faculty of Medicine and General University Hospital Prague Czech Republic
Charles University 2nd Faculty of Medicine and University Hospital Motol Prague Czech Republic
Children's Nebraska University of Nebraska Medical Center Omaha NE USA
Department of Clinical Genetics Cook Children's Hospital Fort Worth TX USA
Department of Clinical Genetics Leiden University Medical Center Leiden The Netherlands
Department of Genetics University Medical Center Utrecht Netherlands
Department of Human Genetics Children's Hospital of Philadelphia Philadelphia PA USA
Department of Human Genetics Inselspital Bern University of Bern Bern Switzerland
Department of Molecular and Human Genetics Baylor College of Medicine Houston TX USA
Department of Paediatrics University of Melbourne Melbourne VIC Australia
Department of Pediatric Neurology University Hospital Antwerp Antwerp Belgium
Department of Pediatrics Baylor College of Medicine San Antonio TX USA
Department of Pediatrics Duke University Hospital Durham NC USA
Division of Genetics and Metabolism Massachusetts General Hospital for Children Boston MA USA
Division of Medical Genetics Duke University Hospital Durham NC USA
Division of Pediatric Neurology Duke University Hospital Durham NC USA
DMG Children's Rehabilitative Services Phoenix AZ USA
Genetics Department Mary Bridge Children's Hospital Multicare Health System Tacoma WA USA
Greenwood Genetic Center Greenwood SC USA
Harvard Medical School Boston MA USA
Institute of Human Genetics Heinrich Heine University Düsseldorf Medical Faculty Düsseldorf Germany
Institute of Human Genetics University of Leipzig Medical Center Leipzig Germany
Laboratoire de Biologie Médicale Multi Sites SeqOIA Paris France
McMaster University Medical Centre Hamilton ON Canada
Medical genetics department Centre Hospitalier Le Mans France
Medical Genetics Department University Hedi Chaker Hospital of Sfax Sfax Tunisia
Medicine Genetics Group Vall Hebron Research Institute Barcelona Spain
Nemours Children's Health Wilmington DE USA
NEURO Research Centre of Excellence University of Antwerp Antwerp Belgium
Orlando Health Arnold Palmer Hospital For Children Orlando FL USA
Perelman School of Medicine University of Pennsylvania Philadelphia PA USA
Service de Génétique CHU de Tours Tours France
Service de Génétique médicale Centre Labellisé Anomalies du Développement Ouest Site Poitiers France
Service de Génétique Médicale CHU d'Angers Angers France
Shodair Children's Hospital Helena MT USA
Tasmanian Clinical Genetics Service Tasmanian Health Service Hobart TAS Australia
UCL Great Ormond Street Institute of Child Health London UK
UMR1253 iBrain Inserm University of Tours Tours France
University of Calgary Calgary AB Canada
University of Utah Salt Lake City UT USA
University of Western Ontario London ON Canada
Victorian Clinical Genetics Services Murdoch Children's Research Institute Parkville VIC Australia
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