Works matching IS 10452257 AND DT 1997 AND VI 19 AND IP 4
Results: 13
Genetic lesions associated with blastic transformation of polycythemia vera and essential thrombocythemia.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 250, doi. 10.1002/(SICI)1098-2264(199708)19:4<250::AID-GCC7>3.0.CO;2-W
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Frequent loss of the 11q14-24 region in chronic lymphocytic leukemia: A study by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 286, doi. 10.1002/(SICI)1098-2264(199708)19:4<286::AID-GCC12>3.0.CO;2-E
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Variable FHIT transcripts in non-neoplastic tissues.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 215, doi. 10.1002/(SICI)1098-2264(199708)19:4<215::AID-GCC2>3.0.CO;2-#
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Linkage analysis of familial melanoma and chromosome 6 in 14 Australian kindreds.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 241, doi. 10.1002/(SICI)1098-2264(199708)19:4<241::AID-GCC6>3.0.CO;2-X
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Increased chromosome 20 copy number detected by fluorescence in situ hybridization (FISH) in malignant melanoma.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 278, doi. 10.1002/(SICI)1098-2264(199708)19:4<278::AID-GCC11>3.0.CO;2-C
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Sustained nontumorigenic phenotype correlates with a largely stable chromosome content during long-term culture of the human keratinocyte line HaCaT.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 201, doi. 10.1002/(SICI)1098-2264(199708)19:4<201::AID-GCC1>3.0.CO;2-0
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Advanced-stage cervical carcinomas are defined by a recurrent pattern of chromosomal aberrations revealing high genetic instability and a consistent gain of chromosome arm 3q.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 233, doi. 10.1002/(SICI)1098-2264(199708)19:4<233::AID-GCC5>3.0.CO;2-Y
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Genetic alterations in primary breast cancers and their metastases: Direct comparison using modified comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 267, doi. 10.1002/(SICI)1098-2264(199708)19:4<267::AID-GCC9>3.0.CO;2-V
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FISH analysis of translocations involving the short arm of chromosome 9 in lymphoid malignancies.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 273, doi. 10.1002/(SICI)1098-2264(199708)19:4<273::AID-GCC10>3.0.CO;2-H
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Analysis of multiple renal cell adenomas and carcinomas suggests allelic loss at 3p21 to be a prerequisite for malignant development.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 228, doi. 10.1002/(SICI)1098-2264(199708)19:4<228::AID-GCC4>3.0.CO;2-Z
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Differential splicing of exon 5 of the Wilms tumour ( WT1) gene.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 256, doi. 10.1002/(SICI)1098-2264(199708)19:4<256::AID-GCC8>3.0.CO;2-W
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The first recurring chromosome translocation in hepatoblastoma: Der(4)t(1;4)(q12;q34).
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 291, doi. 10.1002/(SICI)1098-2264(199708)19:4<291::AID-GCC13>3.0.CO;2-J
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Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 220, doi. 10.1002/(SICI)1098-2264(199708)19:4<220::AID-GCC3>3.0.CO;2-Z
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