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Current Molecular Medicine|March 20, 2002
Restoring the phenotype of fragile X syndrome: insight from the mouse modelI Gantois, C E Bakker, E Reyniers, et al.Archives of Neurology|March 12, 2008
Maternal transmission of multiple sclerosis in a dutch populationIlse A Hoppenbrouwers, Fan Liu, Yurii S Aulchenko, et al.Proceedings of the National Academy of Sciences of the United States of America|May 13, 1997
Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficitsT A Comery, J B Harris, P J Willems, et al.Neurogenetics|December 6, 2005
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern BrazilHsin F Chien, Christan F Rohé, Maria D L Costa, et al.Experimental Cell Research|July 27, 2000
Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouseC E Bakker, Y de Diego Otero, C Bontekoe, et al.Journal of Immunology (Baltimore, Md. : 1950)|January 21, 2012
The IL-7Rα pathway is quantitatively and functionally altered in CD8 T cells in multiple sclerosisKarim L Kreft, Evert Verbraak, Annet F Wierenga-Wolf, et al.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.American Journal of Medical Genetics|May 20, 1999
FMRP expression as a potential prognostic indicator in fragile X syndromeF Tassone, R J Hagerman, D N Iklé, et al.Genomics|April 1, 1992
Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromesC J Faust, A J Verkerk, P J Wilson, et al.Journal of Medical Genetics|December 1, 1994
Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneityP Heutink, T Haitjema, G J Breedveld, et al.Pageof 51