Works matching IS 10452257 AND DT 2013 AND VI 52 AND IP 9
Results: 9
Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization are complementary techniques to detect cytogenetic abnormalities in multiple myeloma.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 785, doi. 10.1002/gcc.22074
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- Article
An analysis of measures of effect size by age of onset in cancer genomewide association studies.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 855, doi. 10.1002/gcc.22081
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- Article
Common chromosomal fragile site FRA16D tumor suppressor WWOX gene expression and metabolic reprograming in cells.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 823, doi. 10.1002/gcc.22078
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- Article
EPCAM germline and somatic rearrangements in lynch syndrome: identification of a novel 3′ EPCAM deletion.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 845, doi. 10.1002/gcc.22080
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- Article
Identification of a novel t(7;14) translocation in multiple myeloma resulting in overexpression of EGFR.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 817, doi. 10.1002/gcc.22077
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- Article
Genome-wide identification of genes with amplification and/or fusion in small cell lung cancer.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 802, doi. 10.1002/gcc.22076
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- Article
An integrated genomic, transcriptional and protein investigation of FGFRL1 as a putative 4p16.3 deletion target in bladder cancer.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 860, doi. 10.1002/gcc.22082
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- Article
Copy neutral loss of heterozygosity is more frequent in older ovarian cancer patients.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 794, doi. 10.1002/gcc.22075
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- Publication type:
- Article
Genetic instability of the tumor suppressor gene FHIT in normal human cells.
- Published in:
- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 832, doi. 10.1002/gcc.22079
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- Article