Works matching IS 10452257 AND DT 2003 AND VI 38 AND IP 3
Results: 12
Pattern of secondary genomic changes in pancreatic tumors of Tgfα/Trp53<sup>+/-</sup> transgenic mice.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 240, doi. 10.1002/gcc.10285
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- Article
CDKN2A as a uveal and cutaneous melanoma susceptibility gene.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 265
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- Article
Development of a real-time RT-PCR assay for the quantification of the most frequent MLL/AF9 fusion types resulting from translocation t(9;11)(p22;q23) in acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 274, doi. 10.1002/gcc.10284
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Aberrant expression of the LHX4 LIM-homeobox gene caused by t(1;14)(q25;q32) in chronic myelogenous leukemia in biphenotypic blast crisis.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 269, doi. 10.1002/gcc.10283
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Clustering of hypermethylated genes in neuroblastoma.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 226, doi. 10.1002/gcc.10278
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- Article
The role of CSMD1 in head and neck carcinogenesis.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 281, doi. 10.1002/gcc.10279
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Molecular cloning of a constitutional t(7;22) translocation associated with risk of hematological malignancy.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 260, doi. 10.1002/gcc.10277
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Expression profiling targeting chromosomes for tumor classification and prediction of clinical behavior.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 207, doi. 10.1002/gcc.10276
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Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 234, doi. 10.1002/gcc.10275
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Molecular cytogenetic characterization of the KG-1 and KG-1a acute myeloid leukemia cell lines by use of spectral karyotyping and fluorescence in situ hybridization.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 249
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- Article
High-resolution mapping of amplifications and deletions in pediatric osteosarcoma by use of CGH analysis of cDNA microarrays.
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 215, doi. 10.1002/gcc.10273
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Molecular analysis of t(X;11)(q24;q23) in an infant with AML-M4 (GenBank accession numbers of the MLL breakpoint region are AF450279, AY246171, AY246172, and AY246173.).
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- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 253, doi. 10.1002/gcc.10272
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- Article