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M R Hayden

Showing results (51-60 of 342) with videos related to

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Atherosclerosis|October 1, 1987
Insufficient evidence to invoke defects in or around the A-I gene as the cause for familial hypoalphalipoproteinemiaM R Hayden, J J Kastelein, S Langlois
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles)A Semaka, J A Collins, M R Hayden
JAMA|November 3, 1989
Insurance and the presymptomatic diagnosis of delayed-onset diseaseO W Quarrell, M Bloch, M R Hayden
Clinical Genetics|July 3, 1998
The fatal attraction of polyglutamine-containing proteinsA S Hackam, C L Wellington, M R Hayden
Clinical Genetics|August 1, 1985
Age of onset in siblings of persons with juvenile Huntington diseaseM R Hayden, J A Soles, R H Ward
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 2, 1980
The prevalence of Huntington's chorea in South AfricaM R Hayden, J M MacGregor, P H Beighton
Journal of Lipid Research|November 21, 2001
Pivotal role of ABCA1 in reverse cholesterol transport influencing HDL levels and susceptibility to atherosclerosisA D Attie, J P Kastelein, M R Hayden
Nucleic Acids Research|May 11, 1987
A polymorphic DNA probe located to human chromosome 4p16 (D4S62)M R Hayden, J Hewitt, A Maresca, et al.
Human Molecular Genetics|November 5, 1997
Rethinking genotype and phenotype correlations in polyglutamine expansion disordersS E Andrew, Y P Goldberg, M R Hayden
American Journal of Medical Genetics|February 1, 1989
Predictive testing for Huntington disease: I. Description of a pilot project in British ColumbiaS Fox, M Bloch, M Fahy, et al.
Pageof 35

Showing results (51-60 of 342) with videos related to

Sort By:
Pageof 35
Atherosclerosis|October 1, 1987
Insufficient evidence to invoke defects in or around the A-I gene as the cause for familial hypoalphalipoproteinemiaM R Hayden, J J Kastelein, S Langlois
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles)A Semaka, J A Collins, M R Hayden
JAMA|November 3, 1989
Insurance and the presymptomatic diagnosis of delayed-onset diseaseO W Quarrell, M Bloch, M R Hayden
Clinical Genetics|July 3, 1998
The fatal attraction of polyglutamine-containing proteinsA S Hackam, C L Wellington, M R Hayden
Clinical Genetics|August 1, 1985
Age of onset in siblings of persons with juvenile Huntington diseaseM R Hayden, J A Soles, R H Ward
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 2, 1980
The prevalence of Huntington's chorea in South AfricaM R Hayden, J M MacGregor, P H Beighton
Journal of Lipid Research|November 21, 2001
Pivotal role of ABCA1 in reverse cholesterol transport influencing HDL levels and susceptibility to atherosclerosisA D Attie, J P Kastelein, M R Hayden
Nucleic Acids Research|May 11, 1987
A polymorphic DNA probe located to human chromosome 4p16 (D4S62)M R Hayden, J Hewitt, A Maresca, et al.
Human Molecular Genetics|November 5, 1997
Rethinking genotype and phenotype correlations in polyglutamine expansion disordersS E Andrew, Y P Goldberg, M R Hayden
American Journal of Medical Genetics|February 1, 1989
Predictive testing for Huntington disease: I. Description of a pilot project in British ColumbiaS Fox, M Bloch, M Fahy, et al.
Pageof 35