Found: 16
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Analyses of brain tumor cell lines confirm a simple model of relationships among fluorescence in situ hybridization, DNA index, and comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 311, doi. 10.1002/(SICI)1098-2264(199712)20:4<311::AID-GCC1>3.0.CO;2-4
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Comparative genomic hybridization detects frequent overrepresentation of chromosomal material from 3q26, 8q24, and 20q13 in human ovarian carcinomas.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 320, doi. 10.1002/(SICI)1098-2264(199712)20:4<320::AID-GCC2>3.0.CO;2-3
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Human/mouse microcell hybrid based elimination test reduces the putative tumor suppressor region at 3p21.3 to 1.6 cM.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 329, doi. 10.1002/(SICI)1098-2264(199712)20:4<329::AID-GCC3>3.0.CO;2-3
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Characterization of a hairy cell leukemia-associated 5q13.3 inversion breakpoint.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 337, doi. 10.1002/(SICI)1098-2264(199712)20:4<337::AID-GCC4>3.0.CO;2-2
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Deletion mapping defines three discrete areas of allelic imbalance on chromosome arm 8p in oral and oropharyngeal squamous cell carcinomas.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 347, doi. 10.1002/(SICI)1098-2264(199712)20:4<347::AID-GCC5>3.0.CO;2-1
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Four regions of allelic imbalance on 17q12-qter associated with high-grade breast tumors.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 354, doi. 10.1002/(SICI)1098-2264(199712)20:4<354::AID-GCC6>3.0.CO;2-0
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Molecular analysis of the t(8;14)(q24;q11) chromosomal breakpoint junctions in the T-cell leukemia line MOLT-16.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 363, doi. 10.1002/(SICI)1098-2264(199712)20:4<363::AID-GCC7>3.0.CO;2-#
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Increased copy number at 17q22-q24 by CGH in breast cancer is due to high-level amplification of two separate regions.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 372, doi. 10.1002/(SICI)1098-2264(199712)20:4<372::AID-GCC8>3.0.CO;2-Z
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Allelic loss at BRCA1, BRCA2, and adjacent loci in relation to TP53 abnormality in breast cancer.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 377, doi. 10.1002/(SICI)1098-2264(199712)20:4<377::AID-GCC9>3.0.CO;2-Z
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Comparative genomic hybridization reveals frequent gains of 20q, 8q, 11q, 12p, and 17q, and losses of 18q, 9p, and 15q in pancreatic cancer.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 383, doi. 10.1002/(SICI)1098-2264(199712)20:4<383::AID-GCC10>3.0.CO;2-O
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Hyperdiploidy and E2A-PBX1 fusion in an adult with t(1;19)+ acute lymphoblastic leukemia: Case report and review of the literature.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 392, doi. 10.1002/(SICI)1098-2264(199712)20:4<392::AID-GCC11>3.0.CO;2-P
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Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 399, doi. 10.1002/(SICI)1098-2264(199712)20:4<399::AID-GCC12>3.0.CO;2-I
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Characterization of a t(10;12)(q24;p13) in a case of CML in transformation.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 408, doi. 10.1002/(SICI)1098-2264(199712)20:4<408::AID-GCC13>3.0.CO;2-I
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Detection of chromosomal aberrations in seminomatous germ cell tumours using comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 412, doi. 10.1002/(SICI)1098-2264(199712)20:4<412::AID-GCC14>3.0.CO;2-O
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1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 419, doi. 10.1002/(SICI)1098-2264(199712)20:4<419::AID-GCC15>3.0.CO;2-H
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Der(16)t(1;16)(q21;q13) as a secondary structural aberration in yet a third sarcoma, extraskeletal myxoid chondrosarcoma.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 4, p. 425, doi. 10.1002/(SICI)1098-2264(199712)20:4<425::AID-GCC16>3.0.CO;2-L
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