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M R Hayden

Showing results (111-120 of 342) with videos related to

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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.
Genomics|June 1, 1992
Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3S Andrew, J Theilmann, A Hedrick, 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.
The Pharmacogenomics Journal|October 26, 2016
The global spectrum of protein-coding pharmacogenomic diversityG E B Wright, B Carleton, M R Hayden, et al.
Clinical Genetics|October 31, 2001
The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery diseaseS M Clee, O Loubser, J Collins, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1996
Origin and migration of an Afrikaner founder mutation FHAfrikaner-2 (V408M) causing familial hypercholesterolemiaJ C Defesche, D E Van Diermen, M R Hayden, et al.
Human Molecular Genetics|January 1, 1994
A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testingS E Andrew, Y P Goldberg, J Theilmann, et al.
Journal 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.
Brain Research Bulletin|November 24, 2001
Onset and pre-onset studies to define the Huntington's disease natural historyF Squitieri, M Cannella, P Giallonardo, et al.
Nature Genetics|May 1, 1992
Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's diseaseO Riess, A Noerremoelle, C Collins, et al.
Pageof 35

Showing results (111-120 of 342) with videos related to

Sort By:
Pageof 35
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.
Genomics|June 1, 1992
Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3S Andrew, J Theilmann, A Hedrick, 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.
The Pharmacogenomics Journal|October 26, 2016
The global spectrum of protein-coding pharmacogenomic diversityG E B Wright, B Carleton, M R Hayden, et al.
Clinical Genetics|October 31, 2001
The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery diseaseS M Clee, O Loubser, J Collins, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1996
Origin and migration of an Afrikaner founder mutation FHAfrikaner-2 (V408M) causing familial hypercholesterolemiaJ C Defesche, D E Van Diermen, M R Hayden, et al.
Human Molecular Genetics|January 1, 1994
A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testingS E Andrew, Y P Goldberg, J Theilmann, et al.
Journal 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.
Brain Research Bulletin|November 24, 2001
Onset and pre-onset studies to define the Huntington's disease natural historyF Squitieri, M Cannella, P Giallonardo, et al.
Nature Genetics|May 1, 1992
Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's diseaseO Riess, A Noerremoelle, C Collins, et al.
Pageof 35