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M M Carrasquillo

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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 populationsM 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 hybridsP 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 genesS H Shaw, M M Carrasquillo, C Kashuk, et al.
Genetics|August 1, 1997
Genetic studies of the mouse mutations mahogany and mahoganoidK A Miller, T M Gunn, M M Carrasquillo, et al.
Neurologia I Neurochirurgia Polska|October 10, 2018
Electroencephalogram findings in patients with posterior cortical atrophyE 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 miceD W Threadgill, A Matin, D Yee, et al.
Genome Research|November 3, 2001
High-throughput variation detection and genotyping using microarraysD 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 diseaseA 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 diseaseM I Kamboh, M M Barmada, F Y Demirci, et al.
Translational Psychiatry|July 27, 2012
Genome-wide association study of Alzheimer's diseaseM I Kamboh, F Y Demirci, X Wang, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 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 populationsM 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 hybridsP 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 genesS H Shaw, M M Carrasquillo, C Kashuk, et al.
Genetics|August 1, 1997
Genetic studies of the mouse mutations mahogany and mahoganoidK A Miller, T M Gunn, M M Carrasquillo, et al.
Neurologia I Neurochirurgia Polska|October 10, 2018
Electroencephalogram findings in patients with posterior cortical atrophyE 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 miceD W Threadgill, A Matin, D Yee, et al.
Genome Research|November 3, 2001
High-throughput variation detection and genotyping using microarraysD 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 diseaseA 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 diseaseM I Kamboh, M M Barmada, F Y Demirci, et al.
Translational Psychiatry|July 27, 2012
Genome-wide association study of Alzheimer's diseaseM I Kamboh, F Y Demirci, X Wang, et al.
Pageof 2