Works matching IS 10452257 AND DT 1998 AND VI 21 AND IP 3
Results: 15
Allelic imbalance and cytogenetic deletion of 1p in colorectal adenomas: A target region identified between DIS199 and DIS234.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 185, doi. 10.1002/(SICI)1098-2264(199803)21:3<185::AID-GCC2>3.0.CO;2-W
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Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitution.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 260, doi. 10.1002/(SICI)1098-2264(199803)21:3<260::AID-GCC12>3.0.CO;2-T
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Molecular cytogenetics of primary breast cancer by CGH.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 177, doi. 10.1002/(SICI)1098-2264(199803)21:3<177::AID-GCC1>3.0.CO;2-X
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Identification of new partner chromosomes involved in fusions with the ETV6 (TEL) gene in hematologic malignancies.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 223, doi. 10.1002/(SICI)1098-2264(199803)21:3<223::AID-GCC6>3.0.CO;2-1
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Multiple possible sites of BRAC2 interacting with DNA repair protein RAD51.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 217, doi. 10.1002/(SICI)1098-2264(199803)21:3<217::AID-GCC5>3.0.CO;2-2
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The second ETV6 allele is not necessarily deleted in acute leukemias with a ETV6/ABL fusion.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 256, doi. 10.1002/(SICI)1098-2264(199803)21:3<256::AID-GCC11>3.0.CO;2-N
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Identification of missense and truncating mutations in the BRCA1 gene in sporadic and familial breast and ovarian cancer.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 244, doi. 10.1002/(SICI)1098-2264(199803)21:3<244::AID-GCC9>3.0.CO;2-#
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Mutations in the human homologue of the Drosophila patched gene in esophageal squamous cell carcinoma.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 276, doi. 10.1002/(SICI)1098-2264(199803)21:3<276::AID-GCC15>3.0.CO;2-N
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Screening for loss of heterozygosity and microsatellite instability in oligodendrogliomas.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 207, doi. 10.1002/(SICI)1098-2264(199803)21:3<207::AID-GCC4>3.0.CO;2-3
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Follicular thyroid carcinoma: Chromosome analysis of 19 cases.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 250, doi. 10.1002/(SICI)1098-2264(199803)21:3<250::AID-GCC10>3.0.CO;2-T
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Homozygous deletion and frequent allelic loss of the 21q11.1-q21.1 region including the ANA gene in human lung carcinoma.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 236, doi. 10.1002/(SICI)1098-2264(199803)21:3<236::AID-GCC8>3.0.CO;2-0
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RAS mutations in pediatric leukemias with MLL gene rearrangements.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 270, doi. 10.1002/(SICI)1098-2264(199803)21:3<270::AID-GCC14>3.0.CO;2-T
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Genetic analysis of glioblastoma multiforme provides evidence for subgroups within the grade.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 195, doi. 10.1002/(SICI)1098-2264(199803)21:3<195::AID-GCC3>3.0.CO;2-V
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Isolation, mapping, and functional analysis of a novel human cDNA ( BNIP3L) encoding a protein homologous to human NIP3.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 230, doi. 10.1002/(SICI)1098-2264(199803)21:3<230::AID-GCC7>3.0.CO;2-0
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Cytogenetic and molecular analysis of cellular atypical mesoblastic nephroma.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 3, p. 265, doi. 10.1002/(SICI)1098-2264(199803)21:3<265::AID-GCC13>3.0.CO;2-O
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