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Genes, Chromosomes & Cancer
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November 1, 1990
In situ hybridization ascertains the presence of a translocation t(6;11) in an acute monocytic leukemia
J Derré, D Cherif, M Le Coniat, et al.
Cancer Genetics and Cytogenetics
|
February 1, 1995
Translocation (2;3)(p22;q28) is associated with myeloid disorders
R Berger, M Flexor, M Le Coniat, et al.
Genes, Chromosomes & Cancer
|
September 1, 1991
Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities
R Berger, M Le Coniat, J Derré, et al.
Cancer Genetics and Cytogenetics
|
October 15, 1992
Abnormalities of chromosome 18 in myelodysplastic syndromes and secondary leukemia
R Berger, M Le Coniat, J Derré, et al.
Cancer Genetics and Cytogenetics
|
January 1, 1990
Cytogenetic studies of 44 T-cell acute lymphoblastic leukemias
R Berger, M Le Coniat, D Vecchione, et al.
Genomics
|
August 1, 1992
The genes for MHC class II regulatory factors RFX1 and RFX2 are located on the short arm of chromosome 19
L Pugliatti, J Derré, R Berger, et al.
Human Genetics
|
September 1, 1991
The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2-p36.3
O Kemper, J Derré, D Cherif, et al.
Leukemia
|
August 1, 1989
Chromosomal rearrangement on chromosome 11q14-q21 in T cell acute lymphoblastic leukemia
R Berger, M Le Coniat, J Derré, et al.
Genes, Chromosomes & Cancer
|
March 1, 1992
The 11q23 breakpoint in acute leukemia with t(11;19)(q23;p13) is distal to those of t(4;11), t(6;11) and t(9;11)
D Cherif, H Der-Sarkissian, J Derré, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1990
Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11
D Cherif, C Julier, O Delattre, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Genes, Chromosomes & Cancer
|
November 1, 1990
In situ hybridization ascertains the presence of a translocation t(6;11) in an acute monocytic leukemia
J Derré, D Cherif, M Le Coniat, et al.
Cancer Genetics and Cytogenetics
|
February 1, 1995
Translocation (2;3)(p22;q28) is associated with myeloid disorders
R Berger, M Flexor, M Le Coniat, et al.
Genes, Chromosomes & Cancer
|
September 1, 1991
Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities
R Berger, M Le Coniat, J Derré, et al.
Cancer Genetics and Cytogenetics
|
October 15, 1992
Abnormalities of chromosome 18 in myelodysplastic syndromes and secondary leukemia
R Berger, M Le Coniat, J Derré, et al.
Cancer Genetics and Cytogenetics
|
January 1, 1990
Cytogenetic studies of 44 T-cell acute lymphoblastic leukemias
R Berger, M Le Coniat, D Vecchione, et al.
Genomics
|
August 1, 1992
The genes for MHC class II regulatory factors RFX1 and RFX2 are located on the short arm of chromosome 19
L Pugliatti, J Derré, R Berger, et al.
Human Genetics
|
September 1, 1991
The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2-p36.3
O Kemper, J Derré, D Cherif, et al.
Leukemia
|
August 1, 1989
Chromosomal rearrangement on chromosome 11q14-q21 in T cell acute lymphoblastic leukemia
R Berger, M Le Coniat, J Derré, et al.
Genes, Chromosomes & Cancer
|
March 1, 1992
The 11q23 breakpoint in acute leukemia with t(11;19)(q23;p13) is distal to those of t(4;11), t(6;11) and t(9;11)
D Cherif, H Der-Sarkissian, J Derré, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1990
Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11
D Cherif, C Julier, O Delattre, et al.
Page
of 4