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Human Genetics
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February 1, 1988
Further localization of ETS1 indicates that the chromosomal rearrangement in Ewing sarcoma does not occur at fra(11)(q23)
R N Simmers, G R Sutherland
Cancer Genetics and Cytogenetics
|
March 1, 1988
No statistical association between common fragile sites and nonrandom chromosome breakpoints in cancer cells
G R Sutherland, R N Simmers
Cytogenetics and Cell Genetics
|
January 1, 1986
Localization of the human haptoglobin genes distal to the fragile site at 16q22 using in situ hybridization
R N Simmers, I Stupans, G R Sutherland
Science (New York, N.Y.)
|
April 3, 1987
Fragile sites at 16q22 are not at the breakpoint of the chromosomal rearrangement in AMMoL
R N Simmers, G R Sutherland, A West, et al.
Human Genetics
|
October 1, 1987
Localization of the human multiple drug resistance gene, MDR1, to 7q21.1
D F Callen, E Baker, R N Simmers, et al.
Journal of Medical Genetics
|
December 1, 1987
Mapping the human alpha globin gene complex to 16p13.2----pter
R N Simmers, J C Mulley, V J Hyland, et al.
Genomics
|
February 1, 1988
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16
D F Callen, V J Hyland, E G Baker, et al.
Cytogenetics and Cell Genetics
|
January 1, 1986
A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) loci
A Fratini, R N Simmers, D F Callen, et al.
Blood
|
July 1, 1987
Localization of the G-CSF gene on chromosome 17 proximal to the breakpoint in the t(15;17) in acute promyelocytic leukemia
R N Simmers, L M Webber, M F Shannon, et al.
Human Genetics
|
February 1, 1988
Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemia
R N Simmers, J Smith, M F Shannon, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Human Genetics
|
February 1, 1988
Further localization of ETS1 indicates that the chromosomal rearrangement in Ewing sarcoma does not occur at fra(11)(q23)
R N Simmers, G R Sutherland
Cancer Genetics and Cytogenetics
|
March 1, 1988
No statistical association between common fragile sites and nonrandom chromosome breakpoints in cancer cells
G R Sutherland, R N Simmers
Cytogenetics and Cell Genetics
|
January 1, 1986
Localization of the human haptoglobin genes distal to the fragile site at 16q22 using in situ hybridization
R N Simmers, I Stupans, G R Sutherland
Science (New York, N.Y.)
|
April 3, 1987
Fragile sites at 16q22 are not at the breakpoint of the chromosomal rearrangement in AMMoL
R N Simmers, G R Sutherland, A West, et al.
Human Genetics
|
October 1, 1987
Localization of the human multiple drug resistance gene, MDR1, to 7q21.1
D F Callen, E Baker, R N Simmers, et al.
Journal of Medical Genetics
|
December 1, 1987
Mapping the human alpha globin gene complex to 16p13.2----pter
R N Simmers, J C Mulley, V J Hyland, et al.
Genomics
|
February 1, 1988
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16
D F Callen, V J Hyland, E G Baker, et al.
Cytogenetics and Cell Genetics
|
January 1, 1986
A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) loci
A Fratini, R N Simmers, D F Callen, et al.
Blood
|
July 1, 1987
Localization of the G-CSF gene on chromosome 17 proximal to the breakpoint in the t(15;17) in acute promyelocytic leukemia
R N Simmers, L M Webber, M F Shannon, et al.
Human Genetics
|
February 1, 1988
Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemia
R N Simmers, J Smith, M F Shannon, et al.
Page
of 1