Found: 15
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Detection of t(11;14) using interphase molecular cytogenetics in mantle cell lymphoma and atypical chronic lymphocytic leukemia.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 175, doi. 10.1002/(SICI)1098-2264(199810)23:2<175::AID-GCC11>3.0.CO;2-N
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Cytogenetic analysis of pancreatic carcinomas: Intratumor heterogeneity and nonrandom pattern of chromosome aberrations.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 81, doi. 10.1002/(SICI)1098-2264(199810)23:2<81::AID-GCC1>3.0.CO;2-0
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MYCN Is the only highly expressed gene from the core amplified domain in human neuroblastomas.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 134, doi. 10.1002/(SICI)1098-2264(199810)23:2<134::AID-GCC6>3.0.CO;2-3
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Masked t(X;18)(p11;q11) in a biphasic synovial sarcoma revealed by FISH and RT-PCR.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 198, doi. 10.1002/(SICI)1098-2264(199810)23:2<198::AID-GCC15>3.0.CO;2-K
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Evidence for a putative telomerase repressor gene in the 3p14.2-p21.1 region.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 123, doi. 10.1002/(SICI)1098-2264(199810)23:2<123::AID-GCC5>3.0.CO;2-4
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Mutation of the mismatch repair gene hMSH2 and hMSH6 in a human T-cell leukemia line tolerant to methylating agents.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 159, doi. 10.1002/(SICI)1098-2264(199810)23:2<159::AID-GCC9>3.0.CO;2-1
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Alveolar soft-part sarcoma: Further evidence by FISH for the involvement of chromosome band 17q25.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 194, doi. 10.1002/(SICI)1098-2264(199810)23:2<194::AID-GCC14>3.0.CO;2-O
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Chromosomal changes during progression of transitional cell carcinoma of the bladder and delineation of the amplified interval on chromosome arm 8q.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 167, doi. 10.1002/(SICI)1098-2264(199810)23:2<167::AID-GCC10>3.0.CO;2-L
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Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 116, doi. 10.1002/(SICI)1098-2264(199810)23:2<116::AID-GCC4>3.0.CO;2-5
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Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomas.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 187, doi. 10.1002/(SICI)1098-2264(199810)23:2<187::AID-GCC13>3.0.CO;2-L
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Dynamics of genetic alterations associated with glioma recurrence.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 153, doi. 10.1002/(SICI)1098-2264(199810)23:2<153::AID-GCC8>3.0.CO;2-1
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A two-color BCR- ABL probe that greatly reduces the false positive and false negative rates for fluorescence in situ hybridization in chronic myeloid leukemia.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 109, doi. 10.1002/(SICI)1098-2264(199810)23:2<109::AID-GCC3>3.0.CO;2-6
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Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 141, doi. 10.1002/(SICI)1098-2264(199810)23:2<141::AID-GCC7>3.0.CO;2-2
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Characterization of recurrent homogeneously staining regions in 72 breast carcinomas.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 100, doi. 10.1002/(SICI)1098-2264(199810)23:2<100::AID-GCC2>3.0.CO;2-6
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Chromosome band 1q21 is recurrently gained in desmoid tumors.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 2, p. 183, doi. 10.1002/(SICI)1098-2264(199810)23:2<183::AID-GCC12>3.0.CO;2-P
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