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Human Genetics|January 1, 1996
Mean corpuscular hemoglobin is not increased in Fmr1 knockout miceE Reyniers, D R Van Bockstaele, K De Boulle, et al.Human Molecular Genetics|October 1, 1992
Segregation of the fragile X mutation from an affected male to his normal daughterP J Willems, B Van Roy, K De Boulle, et al.Genomics|February 28, 1998
Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene familyW Van Hul, W Wuyts, J Hendrickx, 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.Nature Genetics|July 1, 1994
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAML Vits, G Van Camp, P Coucke, et al.Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.European Journal of Human Genetics : EJHG|February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2W Wuyts, W Van Hul, J Hendrickx, et al.American Journal of Medical Genetics|August 9, 1996
Long-term potentiation in the hippocampus of fragile X knockout miceJ M Godfraind, E Reyniers, K De Boulle, et al.Human Molecular Genetics|April 1, 1993
Alternative splicing in the fragile X gene FMR1A J Verkerk, E de Graaff, K De Boulle, et al.Nature Genetics|June 1, 1993
The full mutation in the FMR-1 gene of male fragile X patients is absent in their spermE Reyniers, L Vits, K De Boulle, et al.Pageof 3