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Human Molecular Genetics|January 1, 1994
Sequence of the murine Huntington disease gene: evidence for conservation, alternate splicing and polymorphism in a triplet (CCG) repeat [corrected]B Lin, J Nasir, H MacDonald, et al.Archives of Internal Medicine|October 25, 1993
Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemiaJ C Defesche, K L Pricker, M R Hayden, et al.Journal of Lipid Research|August 1, 1996
Reduced cholesteryl ester transfer in plasma of patients with lipoprotein lipase deficiencyJ D Bagdade, M C Ritter, H Lithell, et al.Genomics|November 15, 1994
Murine alpha-L-iduronidase: cDNA isolation and expressionL A Clarke, J Nasir, H Zhang, et al.Genomics|February 10, 1995
Structural analysis of the 5' region of mouse and human Huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphismsB Lin, J Nasir, M A Kalchman, et al.American Journal of Medical Genetics|June 1, 1986
Cyclopia as a result of an unbalanced familial translocation, rcp(7;18)(q34;q21)R D Smart, J Ross, G Amann, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|March 4, 1998
Phenotypic variation in heterozygous familial hypercholesterolemia: a comparison of Chinese patients with the same or similar mutations in the LDL receptor gene in China or CanadaS N Pimstone, X M Sun, C du Souich, et al.American Journal of Human Genetics|April 1, 1997
Different mechanisms underlie DNA instability in Huntington disease and colorectal cancerG M Goellner, D Tester, S Thibodeau, et al.American Journal of Medical Genetics|August 1, 1986
Restrictive dermopathy: a newly recognized autosomal recessive skin dysplasiaD R Witt, M R Hayden, K A Holbrook, et al.Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 1, 1990
Characterization of a lipoprotein lipase class III type defect in hypertriglyceridemic catsL N Peritz, J D Brunzell, C Harvey-Clarke, et al.Pageof 34