L. P. Kuyt

Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa

A. J. Tipping, Tommy Pearson, Neil V. Morgan et al. · Proceedings of the National Academy of Sciences · 2001 · 122 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A Second Gene for Autosomal Dominant Möbius Syndrome Is Localized to Chromosome 10q, in a Dutch Family

H. T. F. M. Verzijl, Bellinda van den Helm, Bert Veldman et al. · The American Journal of Human Genetics · 1999 · 106 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree.

Peter de Knijff, Arn M. J. M. van den Maagdenberg, A.F.H. Stalenhoef et al. · Journal of Clinical Investigation · 1991 · 100 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Riboflavin-responsive complex I deficiency

H. R. Scholte, H. F. M. Busch, H. D. Bakker et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1995 · 81 citations · Full text

Public Health, Molecular Biology, Micronutrient Deficiency +7

Paracentric inversion inv(11) (q21q23) in the Netherlands

K. Madan, M.H.E.C. Pieters, L. P. Kuyt et al. · Human Genetics · 1990 · 16 citations

Education, Radiology, Projection Mapping +3