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The Netherlands Journal of Medicine|February 1, 1993
The familial hyperchylomicronaemia syndromeS M Bijvoet, T Bruin, J J KasteleinJournal of Medical Genetics|August 1, 1994
Apolipoprotein CII-Padova (Tyr37-->stop) as a cause of chylomicronaemia in an Italian kindred from SiculianaS Tuzgöl, S M Bijvoet, T Bruin, et al.Human Genetics|March 1, 1994
Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descentS M Bijvoet, T Bruin, S Tuzgöl, et al.American Journal of Medical Genetics|August 26, 1998
Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo eventH E Henderson, S M Bijvoet, M A Mannens, et al.The Netherlands Journal of Medicine|November 1, 1996
Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiencyS M Bijvoet, H Wiebusch, Y Ma, et al.Human Molecular Genetics|September 1, 1995
A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemiaP W Reymer, B E Groenemeyer, E Gagné, et al.Pageof 1