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European Journal of Human Genetics : EJHG|January 1, 1995
CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1E Fransen, V Lemmon, G Van Camp, et al.Human Genetics|November 1, 1994
Apparent regression of the CGG repeat in FMR1 to an allele of normal sizeL Vits, K De Boulle, E Reyniers, et al.American Journal of Human Genetics|April 1, 1994
Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in spermG Jansen, P Willems, M Coerwinkel, et al.Nature Genetics|August 1, 1993
A duplication in the L1CAM gene associated with X-linked hydrocephalusG Van Camp, L Vits, P Coucke, et al.American Journal of Human Genetics|October 16, 1999
A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11E Reyniers, P Van Bogaert, N Peeters, 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.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.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.Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.American Journal of Human Genetics|August 1, 1992
Further localization of X-linked hydrocephalus in the chromosomal region Xq28P J Willems, L Vits, P Raeymaekers, et al.Pageof 3