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European Journal of Human Genetics : EJHG|January 1, 1994
Limited expansion of the (CAG)n repeat of the Huntington gene: a premutation (?)E Legius, H Cuppens, H Dierick, et al.
Neurology|May 16, 2002
Familial temporal lobe epilepsy with febrile seizuresC Depondt, W Van Paesschen, G Matthijs, et al.
FEBS Letters|July 1, 1999
Effect of mutations found in carbohydrate-deficient glycoprotein syndrome type IA on the activity of phosphomannomutase 2M Pirard, G Matthijs, L Heykants, et al.
Neurology|November 1, 1996
D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosisW Robberecht, T Aguirre, L Van den Bosch, et al.
Genomics|February 15, 1997
PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13G Matthijs, E Schollen, M Pirard, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Prenatal diagnosis in CDG1 families: beware of heterogeneityG Matthijs, E Schollen, J J Cassiman, et al.
Diabetologia|August 1, 1994
Association of particular HLA class II alleles, haplotypes and genotypes with susceptibility to IDDM in the Belgian populationI Buyse, L A Sandkuyl, M Zamani Ghabanbasani, et al.
Leukemia Research|May 6, 1999
Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH studyD Falzetti, J R Vermeesch, T L Hood, et al.
Human Mutation|May 29, 1998
Fluorescent chemical cleavage of mismatches for efficient screening of the factor VIII geneK Freson, K Peerlinck, T Aguirre, et al.
Leukemia|June 10, 2005
FOXP1, a gene highly expressed in a subset of diffuse large B-cell lymphoma, is recurrently targeted by genomic aberrationsI Wlodarska, E Veyt, P De Paepe, et al.
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