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European Journal of Gastroenterology & Hepatology|September 21, 2001
Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis CH Van Vlierberghe, J R Delanghe, S De Bie, et al.Human Genetics|August 15, 2000
Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IVA De Vos, K Sermon, H Van de Velde, et al.American Journal of Medical Genetics|December 1, 1991
Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridizationF Speleman, J G Leroy, N Van Roy, et al.Cytogenetics and Cell Genetics|November 27, 1999
Refined physical mapping and genomic structure of the EXTL1 geneW Wuyts, N Spieker, N Van Roy, et al.Journal of Medical Genetics|December 18, 2008
Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylationA Willaert, F Malfait, S Symoens, et al.Genes, Chromosomes & Cancer|September 11, 2001
Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell linesN Van Roy, H Van Limbergen, J Vandesompele, et al.Journal of Medical Genetics|February 1, 1990
Linkage data for Marfan syndrome and markers on chromosomes 1 and 11J de Groote, P A Farndon, M V Kilpatrick, et al.American Journal of Medical Genetics|January 1, 1991
Pseudoxanthoma elasticum: similar autosomal recessive subtype in Belgian and Afrikaner familiesA De Paepe, D Viljoen, M Matton, et al.American Journal of Medical Genetics|July 9, 1999
CAG repeat contraction in the androgen receptor gene in three brothers with mental retardationR F Kooy, E Reyniers, K Storm, et al.American Journal of Medical Genetics. Part A|February 4, 2012
Superior mesenteric artery aneurysm in a 9-year-old boy with classical Ehlers-Danlos syndromeK de Leeuw, J F Goorhuis, I F J Tielliu, et al.Pageof 15