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American Journal of Human Genetics|July 1, 1988
Characterization of six partial deletions in the low-density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH)S Langlois, J J Kastelein, M R HaydenLancet (London, England)|June 6, 1987
First-trimester prenatal diagnosis for Huntington's disease with DNA probesM R Hayden, J Hewitt, J J Kastelein, et al.American Journal of Human Genetics|January 1, 1988
A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease geneM R Hayden, J Hewitt, J J Wasmuth, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiencyS Langlois, S Deeb, J D Brunzell, et al.American Journal of Human Genetics|September 1, 1986
Subregional assignment of the linked marker G8 (D4S10) for Huntington disease to chromosome 4p16.1-16.3H S Wang, C R Greenberg, J Hewitt, et al.Alzheimer Disease and Associated Disorders|January 1, 1994
Issues in molecular genetic testing of individuals with suspected early-onset familial Alzheimer's diseaseH Karlinsky, A D Sadovnick, M M Burgess, et al.American Journal of Human Genetics|May 1, 1987
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemiasM R Hayden, H Kirk, C Clark, et al.Neurology|September 1, 1987
The combined use of positron emission tomography and DNA polymorphisms for preclinical detection of Huntington's diseaseM R Hayden, J Hewitt, A J Stoessl, et al.Archives of Neurology|July 1, 1988
Presymptomatic neuropsychological impairment in Huntington's diseaseG W Jason, E M Pajurkova, O Suchowersky, et al.Nature|April 21, 1988
A highly polymorphic locus very tightly linked to the Huntington's disease geneJ J Wasmuth, J Hewitt, B Smith, et al.Pageof 114