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Human Molecular Genetics|January 1, 1997
L1-associated diseases: clinical geneticists divide, molecular geneticists uniteE Fransen, G Van Camp, L Vits, et al.American Journal of Medical Genetics|July 12, 1996
The clinical spectrum of mutations in L1, a neuronal cell adhesion moleculeE Fransen, L Vits, G Van Camp, et al.Journal of Medical Genetics|June 4, 1998
Genotype-phenotype correlation in L1 associated diseasesE Fransen, G Van Camp, R D'Hooge, et al.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|July 1, 1992
PCR detection of a BclI RFLP in the G6PD gene of CaucasiansP J Willems, L VitsHuman Genetics|November 1, 1992
BglII RFLP in DXS 498 between the pigment gene repeat unit, RCP and GCPL Vits, P J WillemsBritish Journal of Audiology|July 13, 2000
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?E Fransen, G Van CampNature Genetics|August 1, 1993
A duplication in the L1CAM gene associated with X-linked hydrocephalusG Van Camp, L Vits, P Coucke, et al.Preparative Biochemistry & Biotechnology|August 26, 1998
Dependence of the ligation efficiency of large DNA fragments isolated from agarose gels on the purification methodE Fransen, G Van Camp, B WinnepenninckxNature 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.Pageof 42