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Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 25, 2023
Ocular manifestations in Koolen-de Vries syndrome: an international studyDafna Shalev, David A Koolen, Bert B A de Vries, et al.European Journal of Medical Genetics|June 15, 2016
Duplications of SLC1A3: Associated with ADHD and autismClaudia J M van Amen-Hellebrekers, Sandra Jansen, Rolph Pfundt, et al.American Journal of Medical Genetics. Part A|September 30, 2022
Familial Bainbridge-Ropers syndrome: Report of familial ASXL3 inheritance and a milder phenotypeSchaida Schirwani, Emily Woods, David A Koolen, et al.Journal of Human Genetics|July 26, 2006
Holoprosencephaly and preaxial polydactyly associated with a 1.24 Mb duplication encompassing FBXW11 at 5q35.1David A Koolen, Jos Herbergs, Joris A Veltman, et al.European Journal of Human Genetics : EJHG|February 19, 2021
Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndromeAlexander J M Dingemans, Diante E Stremmelaar, Roos van der Donk, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|November 27, 2022
GenIDA: an international participatory database to gain knowledge on health issues related to genetic forms of neurodevelopmental disordersPauline Burger, Florent Colin, Axelle Strehle, et al.European Journal of Human Genetics : EJHG|January 9, 2014
Variability in dentofacial phenotypes in four families with WNT10A mutationsChristian P Vink, Charlotte W Ockeloen, Sietske ten Kate, et al.American Journal of Medical Genetics. Part A|June 23, 2023
Clinical and radiological assessment of scoliosis in Koolen-de Vries syndromeArianne Bouman, Romy N Bouwmeester, Leo A van Vlimmeren, et al.American Journal of Medical Genetics. Part A|February 14, 2006
Interstitial 2.2 Mb deletion at 9q34 in a patient with mental retardation but without classical features of the 9q subtelomeric deletion syndromeTjitske Kleefstra, David A Koolen, Willy M Nillesen, et al.Developmental Medicine and Child Neurology|May 11, 2007
A novel microdeletion in 1(p34.2p34.3), involving the SLC2A1 (GLUT1) gene, and severe delayed developmentSascha Vermeer, David A Koolen, Gepke Visser, et al.Pageof 9