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Human Molecular Genetics
|
February 3, 2000
The establishment of telomerase-immortalized cell lines representing human chromosome instability syndromes
M M Ouellette, L D McDaniel, W E Wright, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Mapping of the human cardiac Na+/Ca2+ exchanger gene (NCX1) by fluorescent in situ hybridization to chromosome region 2p22-->p23
L D McDaniel, W J Lederer, P Kofuji, et al.
American Journal of Medical Genetics
|
August 5, 2000
Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group
L D McDaniel, R Prueitt, L C Probst, et al.
Genomics
|
February 15, 1997
Construction and screening of a cosmid library generated from a somatic cell hybrid bearing human chromosome 15
L D McDaniel, B Zhang, E Kubiczek, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1991
Functional complementation of ataxia-telangiectasia group D (AT-D) cells by microcell-mediated chromosome transfer and mapping of the AT-D locus to the region 11q22-23
C Lambert, R A Schultz, M Smith, et al.
Nature Genetics
|
December 2, 2000
Cancer predisposition caused by elevated mitotic recombination in Bloom mice
G Luo, I M Santoro, L D McDaniel, et al.
The Journal of Biological Chemistry
|
March 7, 1998
Differential expression of mitochondrial DNA replication factors in mammalian tissues
R A Schultz, S J Swoap, L D McDaniel, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 8, 2015
Diagnostic utility of microarray testing in pregnancy loss
J A Rosenfeld, M E Tucker, L F Escobar, et al.
Cell
|
August 25, 1995
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH
K A Henning, L Li, N Iyer, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Human Molecular Genetics
|
February 3, 2000
The establishment of telomerase-immortalized cell lines representing human chromosome instability syndromes
M M Ouellette, L D McDaniel, W E Wright, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Mapping of the human cardiac Na+/Ca2+ exchanger gene (NCX1) by fluorescent in situ hybridization to chromosome region 2p22-->p23
L D McDaniel, W J Lederer, P Kofuji, et al.
American Journal of Medical Genetics
|
August 5, 2000
Novel assay for Roberts syndrome assigns variable phenotypes to one complementation group
L D McDaniel, R Prueitt, L C Probst, et al.
Genomics
|
February 15, 1997
Construction and screening of a cosmid library generated from a somatic cell hybrid bearing human chromosome 15
L D McDaniel, B Zhang, E Kubiczek, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1991
Functional complementation of ataxia-telangiectasia group D (AT-D) cells by microcell-mediated chromosome transfer and mapping of the AT-D locus to the region 11q22-23
C Lambert, R A Schultz, M Smith, et al.
Nature Genetics
|
December 2, 2000
Cancer predisposition caused by elevated mitotic recombination in Bloom mice
G Luo, I M Santoro, L D McDaniel, et al.
The Journal of Biological Chemistry
|
March 7, 1998
Differential expression of mitochondrial DNA replication factors in mammalian tissues
R A Schultz, S J Swoap, L D McDaniel, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 8, 2015
Diagnostic utility of microarray testing in pregnancy loss
J A Rosenfeld, M E Tucker, L F Escobar, et al.
Cell
|
August 25, 1995
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH
K A Henning, L Li, N Iyer, et al.
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of 2