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- 2003
-
Mark
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).
(
- Contribution to journal › Article
-
Mark
Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies. a multicolor and locus-specific fluorescence in situ hybridization study.
(
- Contribution to journal › Article
- 2002
-
Mark
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.
(
- Contribution to journal › Article
-
Mark
Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
(
- Contribution to journal › Article
- 2001
-
Mark
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)
(
- Contribution to journal › Article
-
Mark
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
(
- Contribution to journal › Article
-
Mark
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL
(
- Contribution to journal › Article
-
Mark
Isodicentric 7p, idic(7)(q11.2), in acute myeloid
(
- Contribution to journal › Article
-
Mark
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH
(
- Contribution to journal › Article
- 1999
-
Mark
Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations
(
- Contribution to journal › Article
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