Works matching IS 10452257 AND DT 1999 AND VI 26 AND IP 2
Results: 13
Genomic imbalances are rare in hairy cell leukemia.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 182, doi. 10.1002/(SICI)1098-2264(199910)26:2<182::AID-GCC13>3.0.CO;2-Z
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A novel chromosomal region of allelic loss, 4q32-q34, in human osteosarcomas revealed by representational difference analysis.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 115, doi. 10.1002/(SICI)1098-2264(199910)26:2<115::AID-GCC3>3.0.CO;2-E
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Chromosome band 9p21 is frequently altered in malignant peripheral nerve sheath tumors: Studies of CDKN2A and other genes of the pRB pathway.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 151, doi. 10.1002/(SICI)1098-2264(199910)26:2<151::AID-GCC7>3.0.CO;2-A
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Leiomyoma-do viruses play the main role?
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 181, doi. 10.1002/(SICI)1098-2264(199910)26:2<181::AID-GCC12>3.0.CO;2-2
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Regional reproducibility of microsatellite instability in sporadic colorectal cancer.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 106, doi. 10.1002/(SICI)1098-2264(199910)26:2<106::AID-GCC2>3.0.CO;2-F
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Characterization of topoisomerase IIα gene amplification and deletion in breast cancer.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 142, doi. 10.1002/(SICI)1098-2264(199910)26:2<142::AID-GCC6>3.0.CO;2-B
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CHK1 frameshift mutations in genetically unstable colorectal and endometrial cancers.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 176, doi. 10.1002/(SICI)1098-2264(199910)26:2<176::AID-GCC11>3.0.CO;2-3
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Nonrandom fusion of L-Plastin(LCP1) and LAZ3(BCL6) genes by t(3;13)(q27;q14) chromosome translocation in two cases of B-cell non-Hodgkin lymphoma.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 97, doi. 10.1002/(SICI)1098-2264(199910)26:2<97::AID-GCC1>3.0.CO;2-9
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Allelic loss at 1p34, 13q12, 17p13.3, and 17q21.1 correlates with poor postoperative prognosis in breast cancer.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 134, doi. 10.1002/(SICI)1098-2264(199910)26:2<134::AID-GCC5>3.0.CO;2-9
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Amplification of the 11q23 region in acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 166, doi. 10.1002/(SICI)1098-2264(199910)26:2<166::AID-GCC9>3.0.CO;2-P
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Homozygous deletion at the 9q32-33 candidate tumor suppressor locus in primary human bladder cancer.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 171, doi. 10.1002/(SICI)1098-2264(199910)26:2<171::AID-GCC10>3.0.CO;2-B
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A high frequency of tumors with rearrangements of genes of the HMGI(Y) family in a series of 191 pulmonary chondroid hamartomas.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 125, doi. 10.1002/(SICI)1098-2264(199910)26:2<125::AID-GCC4>3.0.CO;2-A
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A case of inv(8)(p11q24) associated with acute myeloid leukemia involves the MOZ and CBP genes in a masked t(8;16).
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 2, p. 161, doi. 10.1002/(SICI)1098-2264(199910)26:2<161::AID-GCC8>3.0.CO;2-6
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