Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome

Genes Chromosomes and Cancer

Volumn 36, Issue 2, 2003, Pages 121-128

  Lillington, Debra M ^a,b   Kingston, Judith E ^a   Coen, Pietro G ^a   Price, Elizabeth ^a   Hungerford, John ^a   Domizio, Paola ^a   Young, Bryan D ^a   Onadim, Zerrin ^a  

^a NATIONAL HEALTH SERVICE   (United Kingdom)

^b IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CANCER GROWTH; CHILD; CHROMOSOMAL LOCALIZATION; CHROMOSOME 13Q; CHROMOSOME 16; CHROMOSOME 1Q; CHROMOSOME 5Q; CHROMOSOME 6P; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; DISEASE ASSOCIATION; GENETIC ASSOCIATION; HISTOPATHOLOGY; HUMAN; PRIORITY JOURNAL; PROGNOSIS; RELIABILITY; RETINOBLASTOMA; STATISTICAL SIGNIFICANCE; TREATMENT OUTCOME; TUMOR CLASSIFICATION;

CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 16; DISEASE PROGRESSION; FEMALE; GENE AMPLIFICATION; HUMANS; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; MULTIVARIATE ANALYSIS; NUCLEIC ACID HYBRIDIZATION; RETINAL NEOPLASMS; RETINOBLASTOMA;

EID: 0037299508     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/gcc.10149     Document Type: Article

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