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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 WillemsClinical Genetics|November 15, 2005
An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromasW Wuyts, R Radersma, K Storm, et al.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.Acta Clinica Belgica|July 3, 2016
DNA Diagnosis of Cystic Fibrosis by Direct Detection of the Af508 MutationJ Hendrickx, J Wauters, P Coucke, et al.DTW. Deutsche Tierarztliche Wochenschrift|December 1, 1993
A case of atresia ani with rectovestibular fistulae in an alpaca (L. pacos)C H Del Campo, L Vits, M R Del Campo, et al.Genomics|November 1, 1993
Localization of a gene responsible for nonspecific mental retardation (MRX9) to the pericentromeric region of the X chromosomeP Willems, L Vits, I Buntinx, et al.Acta Clinica Belgica|January 1, 1991
DNA diagnosis of cystic fibrosis by direct detection of the delta F508 mutationJ Hendrickx, J Wauters, P Coucke, et al.Pageof 3