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Clinical Neurology and Neurosurgery|January 1, 1991
Heredo-ataxia in a large Dutch pedigree. M.R.I. findingsW E Vliegenthart, G J Vielvoye, L P Kuyt
Biochimica Et Biophysica Acta|May 24, 1995
Riboflavin-responsive complex I deficiencyH R Scholte, H F Busch, H D Bakker, et al.
American Journal of Human Genetics|August 12, 1999
A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch familyH T Verzijl, B van den Helm, B Veldman, et al.
The Journal of Clinical Investigation|August 1, 1991
Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigreeP de Knijff, A M van den Maagdenberg, A F Stalenhoef, et al.
Human Molecular Genetics|September 1, 1996
Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch familyH Kremer, L P Kuyt, B van den Helm, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2001
Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South AfricaA J Tipping, T Pearson, N V Morgan, et al.
Human Genetics|June 1, 1990
Paracentric inversion inv(11)(q21q23) in The NetherlandsK Madan, M H Pieters, L P Kuyt, et al.
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