Works matching IS 10452257 AND DT 2002 AND VI 34 AND IP 2
Results: 12
Genetic differences detected by comparative genomic hybridization in head and neck squamous cell carcinomas from different tumor sites: construction of oncogenetic trees for tumor progression.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 224, doi. 10.1002/gcc.10062
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- Article
t(1;3)(p36;p21) is a recurring therapy-related translocation.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 186, doi. 10.1002/gcc.10055
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- Article
Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15).
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 249, doi. 10.1002/gcc.10066
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- Article
Defective DNA-mismatch repair: a potential mediator of leukemogenic susceptibility in therapy-related myelodysplasia and leukemia.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 243, doi. 10.1002/gcc.10059
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- Article
Genome profiles of familial/bilateral and sporadic testicular germ cell tumors.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 168, doi. 10.1002/gcc.10058
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- Article
Uncovering novel inter- and intrachromosomal chromosome 1 aberrations in follicular lymphomas by using an innovative multicolor banding technique.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 201, doi. 10.1002/gcc.10069
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- Article
Suppression of the tumorigenic phenotype by chromosome 18 transfer into pancreatic cancer cell lines.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 234, doi. 10.1002/gcc.10060
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- Article
The common fragile site FRA16D and its associated gene WWOX are highly conserved in the mouse at Fra8E1.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 154, doi. 10.1002/gcc.10047
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- Article
Molecular cytogenetic analysis of the breakpoint region at 6q21-22 in T-cell lymphoma/leukemia cell lines.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 175, doi. 10.1002/gcc.10057
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- Article
Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplification.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 211, doi. 10.1002/gcc.10063
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- Article
Heterogenic molecular basis for loss of ABL1-BCR transcription: Deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 193, doi. 10.1002/gcc.10056
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- Article
Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 2, p. 137, doi. 10.1002/gcc.10027
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- Article