Works matching IS 10452257 AND DT 2004 AND VI 41 AND IP 3
Results: 14
Aberrations of breast cancer susceptibility genes occur early in sporadic breast tumors and in acquisition of breast epithelial immortalization.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 214, doi. 10.1002/gcc.20089
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Various types of rearrangements target TLX3 locus in T‐cell acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 243, doi. 10.1002/gcc.20088
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Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 203, doi. 10.1002/gcc.20087
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Molecular cytogenetic characterization of proximal‐type epithelioid sarcoma.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 283, doi. 10.1002/gcc.20086
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Comparative expressed sequence hybridization studies of high‐hyperdiploid childhood acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 191
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Chromosome band 16q22‐linked familial AML: Exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphisms.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 278, doi. 10.1002/gcc.20084
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- Article
Emergence of translocation t(9;11)‐positive leukemia during treatment of childhood acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 291, doi. 10.1002/gcc.20083
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MLL translocations with concurrent 3′ deletions: Interpretation of FISH results.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 266, doi. 10.1002/gcc.20082
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A new complex rearrangement involving the ETV6, LOC115548, and MN1 genes in a case of acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 272, doi. 10.1002/gcc.20081
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High‐resolution 19p13.2–13.3 allelotyping of breast carcinomas demonstrates frequent loss of heterozygosity.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 250, doi. 10.1002/gcc.20080
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Involvement of fumarate hydratase in nonsyndromic uterine leiomyomas: Genetic linkage analysis and FISH studies.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 183, doi. 10.1002/gcc.20079
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MDS/AML‐associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 223, doi. 10.1002/gcc.20078
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Characterization of genomic breakpoints in MLL and CBP in leukemia patients with t(11;16).
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 257, doi. 10.1002/gcc.20077
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- Article
Interstitial deletions including chromosome 3 common eliminated region 1 (C3CER1) prevail in human solid tumors from 10 different tissues.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 232
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- Article