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American Journal of Medical Genetics
|
February 25, 2000
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder
E R Martin, M M Menold, C M Wolpert, et al.
Human Molecular Genetics
|
July 1, 1996
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37
M C Speer, R Tandan, P N Rao, et al.
Journal of Alzheimer'S Disease & Parkinsonism
|
November 28, 2017
Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function
H N Cukier, B K Kunkle, K L Hamilton, et al.
Genomics
|
February 9, 2000
Analysis of association at single nucleotide polymorphisms in the APOE region
E R Martin, J R Gilbert, E H Lai, et al.
Annals of Human Genetics
|
March 6, 2008
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease
L Wang, E R Hauser, S H Shah, et al.
Neuroscience Letters
|
April 13, 2017
Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease
B W Kunkle, R M Carney, M A Kohli, et al.
Genomics
|
November 24, 1999
Genetic studies of autistic disorder and chromosome 7
A Ashley-Koch, C M Wolpert, M M Menold, et al.
Human Molecular Genetics
|
August 25, 2000
Myotilin is mutated in limb girdle muscular dystrophy 1A
M A Hauser, S K Horrigan, P Salmikangas, et al.
American Journal of Human Genetics
|
June 28, 2000
SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease
E R Martin, E H Lai, J R Gilbert, et al.
Neurology
|
June 9, 2004
Apolipoprotein E controls the risk and age at onset of Parkinson disease
Y J Li, M A Hauser, W K Scott, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 104) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics
|
February 25, 2000
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder
E R Martin, M M Menold, C M Wolpert, et al.
Human Molecular Genetics
|
July 1, 1996
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37
M C Speer, R Tandan, P N Rao, et al.
Journal of Alzheimer'S Disease & Parkinsonism
|
November 28, 2017
Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function
H N Cukier, B K Kunkle, K L Hamilton, et al.
Genomics
|
February 9, 2000
Analysis of association at single nucleotide polymorphisms in the APOE region
E R Martin, J R Gilbert, E H Lai, et al.
Annals of Human Genetics
|
March 6, 2008
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease
L Wang, E R Hauser, S H Shah, et al.
Neuroscience Letters
|
April 13, 2017
Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease
B W Kunkle, R M Carney, M A Kohli, et al.
Genomics
|
November 24, 1999
Genetic studies of autistic disorder and chromosome 7
A Ashley-Koch, C M Wolpert, M M Menold, et al.
Human Molecular Genetics
|
August 25, 2000
Myotilin is mutated in limb girdle muscular dystrophy 1A
M A Hauser, S K Horrigan, P Salmikangas, et al.
American Journal of Human Genetics
|
June 28, 2000
SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease
E R Martin, E H Lai, J R Gilbert, et al.
Neurology
|
June 9, 2004
Apolipoprotein E controls the risk and age at onset of Parkinson disease
Y J Li, M A Hauser, W K Scott, et al.
Page
of 11