Found: 9
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Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: Frequent loss of 19p13.3 and gain of 19q13.1-13.2.
- Published in:
- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 8, doi. 10.1002/(SICI)1098-2264(199801)21:1<8::AID-GCC3>3.0.CO;2-5
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- Article
Barrett's oesophagus: Microsatellite analysis provides evidence to support the proposed metaplasia-dysplasia-carcinoma sequence.
- Published in:
- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 49, doi. 10.1002/(SICI)1098-2264(199801)21:1<49::AID-GCC7>3.0.CO;2-8
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- Article
Molecular alterations in the TP53 gene of peripheral blood cells of patients with chronic myeloid leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 2, doi. 10.1002/(SICI)1098-2264(199801)21:1<2::AID-GCC2>3.0.CO;2-5
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- Article
Minimal deletion of 3p13→14.2 associated with immortalization of human uroepithelial cells.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 39, doi. 10.1002/(SICI)1098-2264(199801)21:1<39::AID-GCC6>3.0.CO;2-9
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- Article
Another reason to look for tumor suppressor genes on chromosome 21.
- Published in:
- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 1, doi. 10.1002/(SICI)1098-2264(199801)21:1<1::AID-GCC1>3.0.CO;2-5
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- Article
Chromosome loss with concomitant duplication and recombination both contribute most to loss of heterozygosity in vitro.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 30, doi. 10.1002/(SICI)1098-2264(199801)21:1<30::AID-GCC5>3.0.CO;2-9
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- Article
Characterization of a t(8;13)(p11;q11-12) in an atypical myeloproliferative disorder.
- Published in:
- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 70, doi. 10.1002/(SICI)1098-2264(199801)21:1<70::AID-GCC9>3.0.CO;2-5
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- Article
Refinement of the BCL2/immunoglobulin heavy chain fusion gene in t(14;18)(q32;q21) by polymerase chain reaction amplification for long targets.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 17, doi. 10.1002/(SICI)1098-2264(199801)21:1<17::AID-GCC4>3.0.CO;2-B
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- Article
Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germline PTEN mutation.
- Published in:
- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 61, doi. 10.1002/(SICI)1098-2264(199801)21:1<61::AID-GCC8>3.0.CO;2-6
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- Article