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W C Speed

Showing results (1-10 of 12) with videos related to

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The Journal of Heredity|September 25, 2004
Understanding human DNA sequence variationK K Kidd, A J Pakstis, W C Speed, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Short tandem repeat polymorphism evolution in humansF Calafell, A Shuster, W C Speed, et al.
American Journal of Physical Anthropology|February 13, 1999
Genealogy reconstruction from short tandem repeat genotypes in an Amazonian populationF Calafell, A Shuster, W C Speed, et al.
American Journal of Human Genetics|January 1, 1997
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15E L Grigorenko, F B Wood, M S Meyer, et al.
Molecular Psychiatry|June 25, 2008
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferaseN Mukherjee, K K Kidd, A J Pakstis, et al.
The Pharmacogenomics Journal|July 30, 2008
Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 geneM-Y Lee, N Mukherjee, A J Pakstis, et al.
Alcoholism, Clinical and Experimental Research|June 1, 1996
DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism researchK K Kidd, A J Pakstis, C M Castiglione, et al.
Neurology|August 10, 2007
Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null alleleS Niemann, J E Landers, M J Churchill, et al.
American Journal of Human Genetics|June 19, 1998
A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutationsS A Tishkoff, A Goldman, F Calafell, et al.
American Journal of Human Genetics|December 1, 1995
Evolution of haplotypes at the DRD2 locusC M Castiglione, A S Deinard, W C Speed, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The Journal of Heredity|September 25, 2004
Understanding human DNA sequence variationK K Kidd, A J Pakstis, W C Speed, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Short tandem repeat polymorphism evolution in humansF Calafell, A Shuster, W C Speed, et al.
American Journal of Physical Anthropology|February 13, 1999
Genealogy reconstruction from short tandem repeat genotypes in an Amazonian populationF Calafell, A Shuster, W C Speed, et al.
American Journal of Human Genetics|January 1, 1997
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15E L Grigorenko, F B Wood, M S Meyer, et al.
Molecular Psychiatry|June 25, 2008
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferaseN Mukherjee, K K Kidd, A J Pakstis, et al.
The Pharmacogenomics Journal|July 30, 2008
Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 geneM-Y Lee, N Mukherjee, A J Pakstis, et al.
Alcoholism, Clinical and Experimental Research|June 1, 1996
DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism researchK K Kidd, A J Pakstis, C M Castiglione, et al.
Neurology|August 10, 2007
Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null alleleS Niemann, J E Landers, M J Churchill, et al.
American Journal of Human Genetics|June 19, 1998
A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutationsS A Tishkoff, A Goldman, F Calafell, et al.
American Journal of Human Genetics|December 1, 1995
Evolution of haplotypes at the DRD2 locusC M Castiglione, A S Deinard, W C Speed, et al.
Pageof 2