Works matching IS 10452257 AND DT 1997 AND VI 18 AND IP 1
Results: 9
Evaluation of MYC and chromosome 8 copy number in breast carcinoma by interphase cytogenetics.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 1, doi. 10.1002/(SICI)1098-2264(199701)18:1<1::AID-GCC1>3.0.CO;2-7
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Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 42, doi. 10.1002/(SICI)1098-2264(199701)18:1<42::AID-GCC5>3.0.CO;2-1
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Liu P. Paul, Wijmenga C, Hajra A, Blake TB, Kelley CA, Adelstein RS, Bagg A, Rector J, Cotellingam J, Willman CL, Collins FS (1996) Identification of the chimeric protein product of the CBFB-MYH11 fusion gene in Inv(16) leukemia cells. Genes Chromosom. Cancer 16:77-87, 1996.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 71, doi. 10.1002/(SICI)1098-2264(199701)18:1<71::AID-GCC9>3.0.CO;2-Z
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Alu-polymerase chain reaction genomic fingerprinting technique identifies multiple genetic loci associated with pancreatic tumourigenesis.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 30, doi. 10.1002/(SICI)1098-2264(199701)18:1<30::AID-GCC4>3.0.CO;2-2
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Complexity of 12q13-22 amplicon in liposarcoma: Microsatellite repeat analysis.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 66, doi. 10.1002/(SICI)1098-2264(199701)18:1<66::AID-GCC8>3.0.CO;2-#
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Genomic instability in sporadic colorectal cancer quantitated by inter-simple sequence repeat PCR analysis.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 19, doi. 10.1002/(SICI)1098-2264(199701)18:1<19::AID-GCC3>3.0.CO;2-4
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Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 59, doi. 10.1002/(SICI)1098-2264(199701)18:1<59::AID-GCC7>3.0.CO;2-0
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Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 8, doi. 10.1002/(SICI)1098-2264(199701)18:1<8::AID-GCC2>3.0.CO;2-7
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High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.
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- Genes, Chromosomes & Cancer, 1997, v. 18, n. 1, p. 50, doi. 10.1002/(SICI)1098-2264(199701)18:1<50::AID-GCC6>3.0.CO;2-0
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