Works matching IS 10452257 AND DT 1998 AND VI 21 AND IP 2
Results: 14
Minimal sizes of deletions detected by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 172, doi. 10.1002/(SICI)1098-2264(199802)21:2<172::AID-GCC14>3.0.CO;2-T
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Fish mapping of YAC clones at human chromosomal band 7q31.2: Identification of YACS spanning FRA7G within the common region of LOH in breast and prostate cancer.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 152, doi. 10.1002/(SICI)1098-2264(199802)21:2<152::AID-GCC11>3.0.CO;2-T
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Recurrent chromosome changes in two adult fibrosarcomas.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 119, doi. 10.1002/(SICI)1098-2264(199802)21:2<119::AID-GCC7>3.0.CO;2-3
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Human lymphocyte telomerase is genetically regulated.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 124, doi. 10.1002/(SICI)1098-2264(199802)21:2<124::AID-GCC8>3.0.CO;2-2
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Pre-clinical evaluation of probes to detect t(8;21) AML minimal residual disease by fluorescence in situ hybridization.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 144, doi. 10.1002/(SICI)1098-2264(199802)21:2<144::AID-GCC10>3.0.CO;2-R
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Fluorescence in situ hybridization (FISH) on peripheral blood smears for monitoring Philadelphia chromosome-positive chronic myeloid leukemia (CML) during interferon treatment: A new strategy for remission assessment.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 90, doi. 10.1002/(SICI)1098-2264(199802)21:2<90::AID-GCC3>3.0.CO;2-2
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Determination of the replication error phenotype in human tumors without the requirement for matching normal DNA by analysis of mononucleotide repeat microsatellites.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 101, doi. 10.1002/(SICI)1098-2264(199802)21:2<101::AID-GCC4>3.0.CO;2-4
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Sporadic breast cancers exhibit loss of heterozygosity on chromosome segment 10q23 close to the Cowden disease locus.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 166, doi. 10.1002/(SICI)1098-2264(199802)21:2<166::AID-GCC13>3.0.CO;2-P
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Cytogenetic and molecular analysis of a t(1;22)(p36;q11.2) in a rhabdoid tumor with a putative homozygous deletion of chromosome 22.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 82, doi. 10.1002/(SICI)1098-2264(199802)21:2<82::AID-GCC2>3.0.CO;2-3
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Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 113, doi. 10.1002/(SICI)1098-2264(199802)21:2<113::AID-GCC6>3.0.CO;2-3
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Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 160, doi. 10.1002/(SICI)1098-2264(199802)21:2<160::AID-GCC12>3.0.CO;2-V
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Refinement of the commonly deleted segment in myeloid leukemias with a del(20q).
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 75, doi. 10.1002/(SICI)1098-2264(199802)21:2<75::AID-GCC1>3.0.CO;2-4
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Mapping of a new target region of allelic loss to a 2-cM interval at 22q13.1 in primary breast cancer.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 108, doi. 10.1002/(SICI)1098-2264(199802)21:2<108::AID-GCC5>3.0.CO;2-4
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Prognostic significance of allelic imbalance of chromosome arms 7q, 8p, 16q, and 18q in stage T<sub>3</sub>N<sub>0</sub>M<sub>0</sub> prostate cancer.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 2, p. 131, doi. 10.1002/(SICI)1098-2264(199802)21:2<131::AID-GCC9>3.0.CO;2-1
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