Works matching IS 10452257 AND DT 2014 AND VI 53 AND IP 6
Results: 8
Comprehensive cytogenetic and molecular cytogenetic analysis of 44 Burkitt lymphoma cell lines: Secondary chromosomal changes characterization, karyotypic evolution, and comparison with primary samples.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 497, doi. 10.1002/gcc.22161
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- Article
Complex IGH rearrangements in multiple myeloma: Frequent detection discrepancies among three different probe sets.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 467, doi. 10.1002/gcc.22158
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- Article
Increased frequency of minimal homozygous deletions is associated with poor prognosis in primary malignant melanoma patients.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 487, doi. 10.1002/gcc.22160
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- Article
The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: Haplotype associations and gene-environment interactions.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 454, doi. 10.1002/gcc.22157
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- Article
Frequent translocations of 11q13.2 and 19p13.2 in ovarian cancer.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 447, doi. 10.1002/gcc.22152
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- Article
Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 524, doi. 10.1002/gcc.22163
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- Article
Variants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 516, doi. 10.1002/gcc.22162
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- Article
Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material.
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- Genes, Chromosomes & Cancer, 2014, v. 53, n. 6, p. 475, doi. 10.1002/gcc.22159
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- Article