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Human Molecular Genetics
|
November 5, 1997
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations
M M Carrasquillo, J Zlotogora, S Barges, et al.
Cytogenetics and Cell Genetics
|
May 27, 1999
Assignment of a novel bifurcated SET domain gene, SETDB1, to human chromosome band 1q21 by in situ hybridization and radiation hybrids
P J Harte, W Wu, M M Carrasquillo, et al.
Genome Research
|
March 21, 1998
Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes
S H Shaw, M M Carrasquillo, C Kashuk, et al.
Genetics
|
August 1, 1997
Genetic studies of the mouse mutations mahogany and mahoganoid
K A Miller, T M Gunn, M M Carrasquillo, et al.
Neurologia I Neurochirurgia Polska
|
October 10, 2018
Electroencephalogram findings in patients with posterior cortical atrophy
E D Goldstein, N Ertekin-Taner, A Stephens, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
June 1, 1997
SSLPs to map genetic differences between the 129 inbred strains and closed-colony, random-bred CD-1 mice
D W Threadgill, A Matin, D Yee, et al.
Genome Research
|
November 3, 2001
High-throughput variation detection and genotyping using microarrays
D J Cutler, M E Zwick, M M Carrasquillo, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
September 2, 2004
Genomic variation in multigenic traits: Hirschsprung disease
A S McCallion, E S Emison, C S Kashuk, et al.
Molecular Psychiatry
|
October 19, 2011
Genome-wide association analysis of age-at-onset in Alzheimer's disease
M I Kamboh, M M Barmada, F Y Demirci, et al.
Translational Psychiatry
|
July 27, 2012
Genome-wide association study of Alzheimer's disease
M I Kamboh, F Y Demirci, X Wang, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Human Molecular Genetics
|
November 5, 1997
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations
M M Carrasquillo, J Zlotogora, S Barges, et al.
Cytogenetics and Cell Genetics
|
May 27, 1999
Assignment of a novel bifurcated SET domain gene, SETDB1, to human chromosome band 1q21 by in situ hybridization and radiation hybrids
P J Harte, W Wu, M M Carrasquillo, et al.
Genome Research
|
March 21, 1998
Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes
S H Shaw, M M Carrasquillo, C Kashuk, et al.
Genetics
|
August 1, 1997
Genetic studies of the mouse mutations mahogany and mahoganoid
K A Miller, T M Gunn, M M Carrasquillo, et al.
Neurologia I Neurochirurgia Polska
|
October 10, 2018
Electroencephalogram findings in patients with posterior cortical atrophy
E D Goldstein, N Ertekin-Taner, A Stephens, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
June 1, 1997
SSLPs to map genetic differences between the 129 inbred strains and closed-colony, random-bred CD-1 mice
D W Threadgill, A Matin, D Yee, et al.
Genome Research
|
November 3, 2001
High-throughput variation detection and genotyping using microarrays
D J Cutler, M E Zwick, M M Carrasquillo, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
September 2, 2004
Genomic variation in multigenic traits: Hirschsprung disease
A S McCallion, E S Emison, C S Kashuk, et al.
Molecular Psychiatry
|
October 19, 2011
Genome-wide association analysis of age-at-onset in Alzheimer's disease
M I Kamboh, M M Barmada, F Y Demirci, et al.
Translational Psychiatry
|
July 27, 2012
Genome-wide association study of Alzheimer's disease
M I Kamboh, F Y Demirci, X Wang, et al.
Page
of 2