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Volumn 91, Issue 5, 2001, Pages 680-686
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Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lacking mycn amplification
a,b
e
INSTITUT CURIE
(France)
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Author keywords
11q deletion; 1p deletion; Comparative genomic hybridization; Genetic subgroup; MYCN; Stage 4 neuroblastoma
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Indexed keywords
ARTICLE;
CANCER STAGING;
CHILD;
CHROMOSOME 11Q;
CHROMOSOME 1P;
COMPARATIVE GENOMIC HYBRIDIZATION;
CONTROLLED STUDY;
DISEASE ASSOCIATION;
GENE AMPLIFICATION;
GENE DELETION;
GENE FREQUENCY;
GENETIC ANALYSIS;
GENETIC PREDISPOSITION;
HUMAN;
HUMAN TISSUE;
INFANT;
MAJOR CLINICAL STUDY;
NEUROBLASTOMA;
PRIORITY JOURNAL;
PROGNOSIS;
ADOLESCENT;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOME ABERRATIONS;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 1;
CHROMOSOMES, HUMAN, PAIR 11;
CHROMOSOMES, HUMAN, PAIR 3;
DISEASE-FREE SURVIVAL;
FEMALE;
GENOME, HUMAN;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
INFANT;
MALE;
MODELS, GENETIC;
MULTICENTER STUDIES;
MUTATION;
NEOPLASM METASTASIS;
NEUROBLASTOMA;
NUCLEIC ACID HYBRIDIZATION;
PROGNOSIS;
TIME FACTORS;
TUMOR CELLS, CULTURED;
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EID: 0035283744
PISSN: 00207136
EISSN: None
Source Type: Journal
DOI: 10.1002/1097-0215(200002)9999:9999<::AID-IJC1114>3.0.CO;2-R Document Type: Article |
Times cited : (109)
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References (28)
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