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M R Hayden

Showing results (91-100 of 342) with videos related to

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Nucleic Acids Research|April 11, 1991
A polymorphic DNA marker at the D8S131 locusB Weber, O Riess, C N Kreklywich, et al.
Human Molecular Genetics|January 15, 1999
In vitro evidence for both the nucleus and cytoplasm as subcellular sites of pathogenesis in Huntington's diseaseA S Hackam, R Singaraja, T Zhang, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|August 1, 1994
Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemiaE Gagné, J Genest, H Zhang, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1997
Toward understanding the molecular pathology of Huntington's diseaseC L Wellington, R R Brinkman, J R O'Kusky, et al.
Clinical Genetics|July 22, 2014
Use of genetic technologies to compare medicinesS E Kolitz, F Towfic, I Grossman, et al.
American Journal of Human Genetics|April 17, 1999
A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington diseaseE W Almqvist, M Bloch, R Brinkman, et al.
American Journal of Human Genetics|October 1, 1992
The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosaO Riess, A Noerremoelle, B Weber, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 6, 1987
Molecular genetics and Huntington's disease. The South African situationM R Hayden, J Goldblatt, G Wallis, et al.
Clinical Genetics|February 28, 2004
Predictive testing for persons at risk for homozygosity for CAG expansion in the Huntington disease geneF Squitieri, E W Almqvist, M Cannella, et al.
Clinical Genetics|October 12, 2001
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British ColumbiaE W Almqvist, D S Elterman, P M MacLeod, et al.
Pageof 35

Showing results (91-100 of 342) with videos related to

Sort By:
Pageof 35
Nucleic Acids Research|April 11, 1991
A polymorphic DNA marker at the D8S131 locusB Weber, O Riess, C N Kreklywich, et al.
Human Molecular Genetics|January 15, 1999
In vitro evidence for both the nucleus and cytoplasm as subcellular sites of pathogenesis in Huntington's diseaseA S Hackam, R Singaraja, T Zhang, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|August 1, 1994
Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemiaE Gagné, J Genest, H Zhang, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1997
Toward understanding the molecular pathology of Huntington's diseaseC L Wellington, R R Brinkman, J R O'Kusky, et al.
Clinical Genetics|July 22, 2014
Use of genetic technologies to compare medicinesS E Kolitz, F Towfic, I Grossman, et al.
American Journal of Human Genetics|April 17, 1999
A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington diseaseE W Almqvist, M Bloch, R Brinkman, et al.
American Journal of Human Genetics|October 1, 1992
The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosaO Riess, A Noerremoelle, B Weber, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 6, 1987
Molecular genetics and Huntington's disease. The South African situationM R Hayden, J Goldblatt, G Wallis, et al.
Clinical Genetics|February 28, 2004
Predictive testing for persons at risk for homozygosity for CAG expansion in the Huntington disease geneF Squitieri, E W Almqvist, M Cannella, et al.
Clinical Genetics|October 12, 2001
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British ColumbiaE W Almqvist, D S Elterman, P M MacLeod, et al.
Pageof 35