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Archives of Biochemistry and Biophysics
|
March 21, 1998
Salt-stable complexes of the Escherichia coli RecBCD enzyme bound to double-stranded DNA
M R Gabbidon, V E Rampersaud, D A Julin
Journal of Medical Genetics
|
December 6, 2005
Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs
E Rampersaud, W K Scott, E R Hauser, et al.
Genetic Epidemiology
|
November 11, 2006
Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent-of-origin (POO) effects in the presence of missing parental genotypes when unaffected siblings are available
E Rampersaud, R W Morris, C R Weinberg, et al.
Clinical Genetics
|
April 16, 2003
Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects
E Rampersaud, E C Melvin, D Siegel, et al.
American Journal of Human Genetics
|
February 15, 2001
A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis
R R Allingham, B Seo, E Rampersaud, et al.
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy
R W Tim, J R Gilbert, J M Stajich, et al.
European Journal of Pain (London, England)
|
May 12, 2017
Pain in knee osteoarthritis is associated with variation in the neurokinin 1/substance P receptor (TACR1) gene
S C Warner, D A Walsh, L L Laslett, et al.
Nutrition & Diabetes
|
August 28, 2013
Generalization of adiposity genetic loci to US Hispanic women
M Graff, L Fernández-Rhodes, S Liu, et al.
Journal of Medical Genetics
|
April 16, 2005
Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10
E Rampersaud, A G Bassuk, D S Enterline, et al.
JAMA
|
November 17, 2001
Complete genomic screen in Parkinson disease: evidence for multiple genes
W K Scott, M A Nance, R L Watts, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Archives of Biochemistry and Biophysics
|
March 21, 1998
Salt-stable complexes of the Escherichia coli RecBCD enzyme bound to double-stranded DNA
M R Gabbidon, V E Rampersaud, D A Julin
Journal of Medical Genetics
|
December 6, 2005
Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs
E Rampersaud, W K Scott, E R Hauser, et al.
Genetic Epidemiology
|
November 11, 2006
Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent-of-origin (POO) effects in the presence of missing parental genotypes when unaffected siblings are available
E Rampersaud, R W Morris, C R Weinberg, et al.
Clinical Genetics
|
April 16, 2003
Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects
E Rampersaud, E C Melvin, D Siegel, et al.
American Journal of Human Genetics
|
February 15, 2001
A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis
R R Allingham, B Seo, E Rampersaud, et al.
Journal of Clinical Neuromuscular Disease
|
December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy
R W Tim, J R Gilbert, J M Stajich, et al.
European Journal of Pain (London, England)
|
May 12, 2017
Pain in knee osteoarthritis is associated with variation in the neurokinin 1/substance P receptor (TACR1) gene
S C Warner, D A Walsh, L L Laslett, et al.
Nutrition & Diabetes
|
August 28, 2013
Generalization of adiposity genetic loci to US Hispanic women
M Graff, L Fernández-Rhodes, S Liu, et al.
Journal of Medical Genetics
|
April 16, 2005
Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10
E Rampersaud, A G Bassuk, D S Enterline, et al.
JAMA
|
November 17, 2001
Complete genomic screen in Parkinson disease: evidence for multiple genes
W K Scott, M A Nance, R L Watts, et al.
Page
of 1