Works matching IS 10452257 AND DT 1999 AND VI 24 AND IP 2
Results: 13
Monoclonality and surface lesion-specific microsatellite alterations in premalignant and malignant neoplasia of uterine cervix: a local field effect of genomic instability and clonal evolution.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 127, doi. 10.1002/(SICI)1098-2264(199902)24:2<127::AID-GCC5>3.0.CO;2-8
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Functional and molecular analyses of 10q deletions in human gliomas.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 135, doi. 10.1002/(SICI)1098-2264(199902)24:2<135::AID-GCC6>3.0.CO;2-A
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Simple variant t(8;21) acute myeloid leukemias harbor insertions of the AML1 or ETO genes.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 165, doi. 10.1002/(SICI)1098-2264(199902)24:2<165::AID-GCC12>3.0.CO;2-1
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Molecular mapping of chromosome 2 deletions in murine radiation-induced AML localizes a putative tumor suppressor gene to a 1.0 cM region homologous to human chromosome segment 11p11-12.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 95, doi. 10.1002/(SICI)1098-2264(199902)24:2<95::AID-GCC1>3.0.CO;2-C
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Chromosome 18 breakpoint in t(11;18)(q21;q21) translocation associated with MALT lymphoma is proximal to BCL2 and distal to DCC.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 156, doi. 10.1002/(SICI)1098-2264(199902)24:2<156::AID-GCC9>3.0.CO;2-X
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Abnormal FHIT transcripts found in both lung cancer and normal lung tissue.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 105, doi. 10.1002/(SICI)1098-2264(199902)24:2<105::AID-GCC2>3.0.CO;2-P
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Clonal chromosome abnormalities in a so-called Dupuytren's subungual exostosis.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 162, doi. 10.1002/(SICI)1098-2264(199902)24:2<162::AID-GCC11>3.0.CO;2-7
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Identification of a homozygous deletion at 8p12-21 in a human prostate cancer xenograft.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 119, doi. 10.1002/(SICI)1098-2264(199902)24:2<119::AID-GCC4>3.0.CO;2-6
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MLL is involved in a t(2;11)(p21;q23) in a patient with acute myeloblastic leukemia.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 151, doi. 10.1002/(SICI)1098-2264(199902)24:2<151::AID-GCC8>3.0.CO;2-E
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TP53 gene mutations in plasma DNA of cancer patients.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 160, doi. 10.1002/(SICI)1098-2264(199902)24:2<160::AID-GCC10>3.0.CO;2-C
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Four-color CGH: A new method for quality control of comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 112, doi. 10.1002/(SICI)1098-2264(199902)24:2<112::AID-GCC3>3.0.CO;2-U
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Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma.
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 144, doi. 10.1002/(SICI)1098-2264(199902)24:2<144::AID-GCC7>3.0.CO;2-9
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Is Hmgic rearranged due to cryptic paracentric inversion of 12q in karyotypically normal uterine leiomyomas?
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- Genes, Chromosomes & Cancer, 1999, v. 24, n. 2, p. 172, doi. 10.1002/(SICI)1098-2264(199902)24:2<172::AID-GCC13>3.0.CO;2-Z
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