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Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome
Jeroen K.J. Van Houdt, Beata Anna Nowakowska, Sérgio B. Sousa, Barbera D.C. Van Schaik, Eve Seuntjens, Nelson Avonce, Alejandro Sifrim, Omar A. Abdul-Rahman, Marie José H. Van Den Boogaard, Armand Bottani, Marco Castori, Valérie Cormier-Daire, Matthew A. Deardorff, Isabel Filges, Alan Fryer, Jean Pierre Fryns, Simone Gana, Livia Garavelli, Gabriele Gillessen-Kaesbach, Bryan D. Hall
*Corresponding author for this work
- KU Leuven
- Institute of Psychiatry and Neurology, Warszawa
- Department of Clinical Genetics
- University of London
- Serviço de Genética Médica
- Hospital Pediátrico de Coimbra
- Bioinformatics Laboratory
- University of Amsterdam
- Ghent University
- Division of Medical Genetics
- University of Mississippi
- Utrecht University
- Department of Genetic and Laboratory Medicine
- University Hospital and Medical Faculty
- Department of Molecular Medicine
- La Sapienza University of Rome
- Département de Génétique
- Université Paris Descartes
- Division of Genetics
- University of Pennsylvania
- University of Basel
- University of Liverpool
- Liverpool Women's NHS Foundation Trust
- University of Pavia
- Department of Obstetric and Pediatric
- Azienda Ospedaliera Santa Maria Nuova di Reggio Emilia
- Department of Pediatrics
- University of Kentucky
- Institut für Medizinische Genetik
- Humboldt University of Berlin
- Children's Memorial Health Institute
- Institut fur Humangenetik
- University of Duisburg-Essen
- University of Ottawa
- Department of Pediatrics
- Kennedy-Galton Center
- Northern Ireland Regional Genetics Service
- Belfast Health and Social Care Trust
- Amphia Hospital
- Erasmus University Medical Center
- Service de Génétique Médicale
- Centre Hospitalier Universitaire (CHU) de Bordeaux
- Department of Child Neurology
- Medical University of Silesia
- Clinical Genetics Service
- City Hospital
- University of Groningen
- University of Brussels
- Division of Medical Genetics
- Department of Pediatrics
- Deptartment of Clinical Genetics and Department of Epidemiology
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