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Volumn 86, Issue 6, 2002, Pages 929-939

Genetic abnormalities detected in ependymomas by comparative genomic hybridisation

(10) Carter, M a,b Nicholson, J a,c Ross, F b Crolla, J b Allibone, R d Balaji, V a Perry, R g Walker, D d Gilbertson, R e,f Ellison, D a,e,g

a SOUTHAMPTON GENERAL HOSPITAL (United Kingdom)

b WESSEX REGIONAL GENETICS LABORATORY (United Kingdom)

c ADDENBROOKE S HOSPITAL (United Kingdom)

d QUEEN S MEDICAL CENTRE (United Kingdom)

e ROYAL VICTORIA INFIRMARY (United Kingdom)

f ST JUDE CHILDREN S RESEARCH HOSPITAL (United States)

g NEWCASTLE GENERAL HOSPITAL (United Kingdom)

Author keywords

CGH; Ependymoma; Gain 1q; Intermediate ploidy; Loss 22

Indexed keywords

DNA;

ADOLESCENT; ADULT; AGED; ARTICLE; CANCER ADJUVANT THERAPY; CANCER RADIOTHERAPY; CANCER SURGERY; CHILD; CHROMOSOME 10Q; CHROMOSOME 13; CHROMOSOME 14Q; CHROMOSOME 1Q; CHROMOSOME 22Q; CHROMOSOME 6Q; CHROMOSOME ABERRATION; CHROMOSOME LOSS; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; EPENDYMOMA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; INFANT; INTRACRANIAL TUMOR; KAPLAN MEIER METHOD; MAJOR CLINICAL STUDY; MALE; PLOIDY; PRIORITY JOURNAL; SKULL TUMOR; SPINE TUMOR;

ADOLESCENT; ADULT; AGED; BRAIN NEOPLASMS; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; EPENDYMOMA; FEMALE; HUMANS; INFANT; MALE; MIDDLE AGED; NUCLEIC ACID HYBRIDIZATION; PLOIDIES; SPINAL CORD NEOPLASMS;

EID: 18344376523 PISSN: 00070920 EISSN: None Source Type: Journal
DOI: 10.1038/sj.bjc.6600180 Document Type: Article

Times cited : (145)

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