Interpreting aCGH-defined karyotypic changes in gliomas using copy number status, loss of heterozygosity and allelic ratios

Experimental and Molecular Pathology

Volumn 88, Issue 1, 2010, Pages 82-89

  Cowell, John K ^a   Lo, Ken C ^a   Luce, Jesse ^a   Hawthorn, Lesleyann ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

Author keywords

Amplification; CGH; Copy number; Deletion; Glioma

Indexed keywords

PROTEIN KINASE B GAMMA; PROTEIN SERINE THREONINE KINASE; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN; ZINC FINGER PROTEIN 532;

ARTICLE; CHROMOSOME 1; CHROMOSOME 17; CHROMOSOME 18; CHROMOSOME 19; CHROMOSOME LOSS; COMPARATIVE GENOMIC HYBRIDIZATION; GENE AMPLIFICATION; GENE DELETION; GENETIC GAIN; GLIOMA; HETEROZYGOSITY LOSS; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; KARYOTYPE; PLOIDY; SINGLE NUCLEOTIDE POLYMORPHISM;

ANEUPLOIDY; CHROMOSOME MAPPING; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; DNA, NEOPLASM; GENE DELETION; GLIOMA; HUMANS; LOSS OF HETEROZYGOSITY; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 75049083572     PISSN: 00144800     EISSN: 10960945     Source Type: Journal    
DOI: 10.1016/j.yexmp.2009.09.014     Document Type: Article

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