Works matching IS 10452257 AND DT 2004 AND VI 40 AND IP 3
Results: 11
Genomic aberrations in carcinomas of the uterine corpus.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 229, doi. 10.1002/gcc.20038
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- Article
Two independent RB1-inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient.
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- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 271, doi. 10.1002/gcc.20042
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- Article
High-resolution mapping of amplicons of the short arm of chromosome 1 in two neuroblastoma tumors by microarray-based comparative genomic hybridization.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 266, doi. 10.1002/gcc.20041
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- Article
HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1.
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- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 261, doi. 10.1002/gcc.20040
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- Article
Mapping of a candidate colorectal cancer tumor-suppressor gene to a 900-kilobase region on the short arm of chromosome 8.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 247, doi. 10.1002/gcc.20039
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- Article
Molecular heterogeneity in AML/MDS patients with 3q21q26 rearrangements.
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- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 179, doi. 10.1002/gcc.20033
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- Article
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 218, doi. 10.1002/gcc.20037
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- Article
Reduced dermatopontin expression is a molecular link between uterine leiomyomas and keloids.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 204, doi. 10.1002/gcc.20035
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- Publication type:
- Article
Allele-specific loss of heterozygosity at the DAL-1/4.1B (EPB41L3) tumor-suppressor gene locus in the absence of mutation.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 190, doi. 10.1002/gcc.20034
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- Article
A model for karyotypic evolution in testicular germ cell tumors.
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- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 172, doi. 10.1002/gcc.20032
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- Article
Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 3, p. 165, doi. 10.1002/gcc.20030
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- Article