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Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
Dennis Lal, Patrick May, Eduardo Perez-Palma, Kaitlin E. Samocha, Jack A. Kosmicki, Elise B. Robinson, Rikke S. Møller, Roland Krause, Peter Nürnberg, Sarah Weckhuysen, Peter De Jonghe, Renzo Guerrini, Lisa M. Niestroj, Juliana Du, Carla Marini, James S. Ware, Mitja Kurki, Padhraig Gormley, Sha Tang, Sitao Wu
*Kontaktforfatter
- Cleveland Clinic Foundation
- Massachusetts Institute of Technology
- Massachusetts General Hospital
- University of Cologne
- University of Luxembourg
- Harvard T.H. Chan School of Public Health
- Antwerp University Hospital
- VIB
- Instituut Born-Bunge
- Meyer Children’s University Hospital
- Division of Clinical Genomics
- CeGaT GmbH
- Boston Children's Hospital
- Justus Liebig University Giessen
- University Medical Center Utrecht
- Children's Hospital of Philadelphia
- Eberhard Karls University of Tübingen
- RWTH Aachen University
- University of Pennsylvania
- University of California
- University of Helsinki
- Broad Institute
- Lerner Research Institute
- Wellcome Trust Genome Campus
- Imperial College London
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
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