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Human Molecular Genetics
|
September 1, 1992
(CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16
O Riess, B Weber, M R Hayden
Italian Journal of Neurological Sciences
|
June 1, 1996
Update on genetics of Huntington's disease: availability of direct and accurate predictive test
F Squitieri, G Campanella, M R Hayden
Clinical Genetics
|
January 6, 2011
Adoption and the communication of genetic risk: experiences in Huntington disease
Y Bombard, A Semaka, M R Hayden
Nucleic Acids Research
|
April 11, 1991
A polymorphic DNA marker at the D10S106 locus
B Weber, O Riess, M R Hayden
Current Opinion in Neurology
|
August 1, 1994
The molecular genetics of Huntington's disease
Y P Goldberg, H Telenius, M R Hayden
Biological Psychiatry
|
April 1, 1993
Monoamines and their metabolites in Huntington's disease brain: evidence for decreased catechol-O-methyltransferase activity
E G McGeer, B Kremer, M R Hayden
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 Hayden
Clinical Genetics
|
July 1, 1994
Gene environment interaction and plasma triglyceride levels: the crucial role of lipoprotein lipase
M R Hayden, M S Liu, Y Ma
Human Molecular Genetics
|
January 1, 1996
Huntington disease: new insights into the relationship between CAG expansion and disease
J Nasir, Y P Goldberg, M R Hayden
Journal of Genetic Counseling
|
August 21, 2012
"Grasping the grey": patient understanding and interpretation of an intermediate allele predictive test result for Huntington disease
A Semaka, L G Balneaves, M R Hayden
Page
of 35
Search research articles
Search
Showing results (41-50 of 342) with videos related to
Sort By:
Page
of 35
Human Molecular Genetics
|
September 1, 1992
(CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16
O Riess, B Weber, M R Hayden
Italian Journal of Neurological Sciences
|
June 1, 1996
Update on genetics of Huntington's disease: availability of direct and accurate predictive test
F Squitieri, G Campanella, M R Hayden
Clinical Genetics
|
January 6, 2011
Adoption and the communication of genetic risk: experiences in Huntington disease
Y Bombard, A Semaka, M R Hayden
Nucleic Acids Research
|
April 11, 1991
A polymorphic DNA marker at the D10S106 locus
B Weber, O Riess, M R Hayden
Current Opinion in Neurology
|
August 1, 1994
The molecular genetics of Huntington's disease
Y P Goldberg, H Telenius, M R Hayden
Biological Psychiatry
|
April 1, 1993
Monoamines and their metabolites in Huntington's disease brain: evidence for decreased catechol-O-methyltransferase activity
E G McGeer, B Kremer, M R Hayden
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 Hayden
Clinical Genetics
|
July 1, 1994
Gene environment interaction and plasma triglyceride levels: the crucial role of lipoprotein lipase
M R Hayden, M S Liu, Y Ma
Human Molecular Genetics
|
January 1, 1996
Huntington disease: new insights into the relationship between CAG expansion and disease
J Nasir, Y P Goldberg, M R Hayden
Journal of Genetic Counseling
|
August 21, 2012
"Grasping the grey": patient understanding and interpretation of an intermediate allele predictive test result for Huntington disease
A Semaka, L G Balneaves, M R Hayden
Page
of 35