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Nature Genetics|June 1, 1993
The full mutation in the FMR-1 gene of male fragile X patients is absent in their spermE Reyniers, L Vits, K De Boulle, et al.Clinical Genetics|February 1, 1991
Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patientsJ G Wauters, J Hendrickx, P Coucke, et al.Genomics|October 1, 1990
Assignment of X-linked hydrocephalus to Xq28 by linkage analysisP J Willems, I Dijkstra, B J Van der Auwera, et al.Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.Genomics|April 1, 1991
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22P J Willems, J Hendrickx, B J Van der Auwera, et al.Archives of Neurology|June 1, 1990
Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same familyP J Willems, L Vits, R J Wanders, et al.Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.Pageof 3