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Neurogenetics
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March 25, 2000
The mutation properties of spinal and bulbar muscular atrophy disease alleles
R P Grewal, E P Leeflang, L Zhang, et al.
Journal of the American Chemical Society
|
July 18, 2001
Hydroxylated quantum dots as luminescent probes for in situ hybridization
S Pathak, S K Choi, N Arnheim, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 15, 1992
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues
G A Cortopassi, D Shibata, N W Soong, et al.
The Journal of Biological Chemistry
|
December 10, 1973
Multiple genes for lysozyme in birds. Studies on black swan egg white lysozymes
N Arnheim, A Hindenburg, G S Begg, et al.
American Journal of Human Genetics
|
March 21, 2000
Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping
S Lien, J Szyda, B Schechinger, et al.
Nature Genetics
|
December 1, 1992
Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain
N W Soong, D R Hinton, G Cortopassi, et al.
The Journal of Biological Chemistry
|
May 10, 1972
Amino acid sequence studies on bobwhite quail egg white lysozyme
E M Prager, N Arnheim, G A Mross, et al.
American Journal of Human Genetics
|
November 1, 1992
A new source of polymorphic DNA markers for sperm typing: analysis of microsatellite repeats in single cells
R Hubert, J L Weber, K Schmitt, et al.
Human Mutation
|
January 1, 1995
Analysis of mutational changes at the HLA locus in single human sperm
M M Huang, H A Erlich, M F Goodman, et al.
Neurobiology of Aging
|
November 1, 1996
Mitochondrial DNA deletions are rare in the free radical-rich retinal environment
N W Soong, M H Dang, D R Hinton, et al.
Page
of 14
Search research articles
Search
Showing results (71-80 of 131) with videos related to
Sort By:
Page
of 14
Neurogenetics
|
March 25, 2000
The mutation properties of spinal and bulbar muscular atrophy disease alleles
R P Grewal, E P Leeflang, L Zhang, et al.
Journal of the American Chemical Society
|
July 18, 2001
Hydroxylated quantum dots as luminescent probes for in situ hybridization
S Pathak, S K Choi, N Arnheim, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 15, 1992
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues
G A Cortopassi, D Shibata, N W Soong, et al.
The Journal of Biological Chemistry
|
December 10, 1973
Multiple genes for lysozyme in birds. Studies on black swan egg white lysozymes
N Arnheim, A Hindenburg, G S Begg, et al.
American Journal of Human Genetics
|
March 21, 2000
Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping
S Lien, J Szyda, B Schechinger, et al.
Nature Genetics
|
December 1, 1992
Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain
N W Soong, D R Hinton, G Cortopassi, et al.
The Journal of Biological Chemistry
|
May 10, 1972
Amino acid sequence studies on bobwhite quail egg white lysozyme
E M Prager, N Arnheim, G A Mross, et al.
American Journal of Human Genetics
|
November 1, 1992
A new source of polymorphic DNA markers for sperm typing: analysis of microsatellite repeats in single cells
R Hubert, J L Weber, K Schmitt, et al.
Human Mutation
|
January 1, 1995
Analysis of mutational changes at the HLA locus in single human sperm
M M Huang, H A Erlich, M F Goodman, et al.
Neurobiology of Aging
|
November 1, 1996
Mitochondrial DNA deletions are rare in the free radical-rich retinal environment
N W Soong, M H Dang, D R Hinton, et al.
Page
of 14