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European Journal of Human Genetics : EJHG|October 16, 2003
MECP2 analysis in mentally retarded patients: implications for routine DNA diagnosticsTjitske Kleefstra, Helger G Yntema, Willy M Nillesen, et al.International Journal of Cancer|May 12, 2009
Tumor microvasculature supports proliferation and expansion of glioma-propagating cellsTijana Borovski, Joost J C Verhoeff, Rosemarie ten Cate, et al.Cancer Research|July 14, 1998
Elevated frequencies of benzo(a)pyrene-induced Hprt mutations in internal tissue of XPA-deficient miceS A Bol, H van Steeg, J G Jansen, et al.Oncogene|June 10, 1998
XPA-deficiency in hairless mice causes a shift in skin tumor types and mutational target genes after exposure to low doses of U.V.BA de Vries, R J Berg, S Wijnhoven, et al.European Journal of Medical Genetics|July 11, 2006
European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalitiesI Feenstra, J Fang, D A Koolen, et al.Journal of Rehabilitation Medicine|October 19, 2023
Daily patterns of fatigue after subarachnoid haemorrhage: an ecological momentary assessment studyElisabeth A De Vries, Majanka H Heijenbrok-Kal, Fop Van Kooten, 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.Clinica E Investigacion En Arteriosclerosis : Publicacion Oficial De La Sociedad Espanola De Arteriosclerosis|May 29, 2014
The postprandial situation as a pro-inflammatory conditionMarijke A de Vries, Boudewijn Klop, Silvia A Eskes, et al.European Journal of Human Genetics : EJHG|February 29, 2024
Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel-Van der Aa syndromeClaudio Peter D'Incal, Dale John Annear, Ellen Elinck, et al.Pageof 88