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The American Journal of Physiology
|
April 1, 1989
In situ hybridization of prepro-epidermal growth factor mRNA in the mouse kidney
E C Salido, P H Yen, L J Shapiro, et al.
American Journal of Human Genetics
|
June 1, 1991
Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier
J C Wang, M B Passage, P H Yen, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1993
An evaluation of the inactive mouse X chromosome in somatic cell hybrids
E C Salido, M B Passage, P H Yen, et al.
Cell
|
May 18, 1990
Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements
P H Yen, X M Li, S P Tsai, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1987
Cytogenetic and molecular studies on a recombinant human X chromosome: implications for the spreading of X chromosome inactivation
T Mohandas, R L Geller, P H Yen, et al.
Cell
|
May 22, 1987
Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange
P H Yen, E Allen, B Marsh, et al.
Nature Genetics
|
May 1, 1996
Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts)
E C Salido, X M Li, P H Yen, et al.
Somatic Cell and Molecular Genetics
|
March 1, 1989
X-chromosome inactivation in cultured cells from human chorionic villi
T K Mohandas, M B Passage, J W Williams, et al.
American Journal of Human Genetics
|
September 1, 1992
Role of the pseudoautosomal region in sex-chromosome pairing during male meiosis: meiotic studies in a man with a deletion of distal Xp
T K Mohandas, R M Speed, M B Passage, et al.
Journal of Clinical Microbiology
|
August 2, 2000
Comparison and application of a novel genotyping method, semiautomated primer-specific and mispair extension analysis, and four other genotyping assays for detection of hepatitis C virus mixed-genotype infections
Y W Hu, E Balaskas, M Furione, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
The American Journal of Physiology
|
April 1, 1989
In situ hybridization of prepro-epidermal growth factor mRNA in the mouse kidney
E C Salido, P H Yen, L J Shapiro, et al.
American Journal of Human Genetics
|
June 1, 1991
Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier
J C Wang, M B Passage, P H Yen, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1993
An evaluation of the inactive mouse X chromosome in somatic cell hybrids
E C Salido, M B Passage, P H Yen, et al.
Cell
|
May 18, 1990
Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements
P H Yen, X M Li, S P Tsai, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1987
Cytogenetic and molecular studies on a recombinant human X chromosome: implications for the spreading of X chromosome inactivation
T Mohandas, R L Geller, P H Yen, et al.
Cell
|
May 22, 1987
Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange
P H Yen, E Allen, B Marsh, et al.
Nature Genetics
|
May 1, 1996
Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts)
E C Salido, X M Li, P H Yen, et al.
Somatic Cell and Molecular Genetics
|
March 1, 1989
X-chromosome inactivation in cultured cells from human chorionic villi
T K Mohandas, M B Passage, J W Williams, et al.
American Journal of Human Genetics
|
September 1, 1992
Role of the pseudoautosomal region in sex-chromosome pairing during male meiosis: meiotic studies in a man with a deletion of distal Xp
T K Mohandas, R M Speed, M B Passage, et al.
Journal of Clinical Microbiology
|
August 2, 2000
Comparison and application of a novel genotyping method, semiautomated primer-specific and mispair extension analysis, and four other genotyping assays for detection of hepatitis C virus mixed-genotype infections
Y W Hu, E Balaskas, M Furione, et al.
Page
of 5