Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics

Cancer Genetics and Cytogenetics

Volumn 130, Issue 1, 2001, Pages 79-83

  Granzow, Martin ^a   Popp, Susanne ^a,b   Weber, Susanne ^a   Schoell, Brigitte ^a   Holtgreve Grez, Heidi ^a   Senf, Leonore ^a   Hager, Dieter ^a   Boschert, Jürgen ^a   Scheurlen, Wolfram ^a   Jauch, Anna ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CISPLATIN; ETOPOSIDE; IFOSFAMIDE; METHOTREXATE; VINCRISTINE;

ARTICLE; BRAIN TUMOR; CASE REPORT; CHILDHOOD; CHROMOSOME 17P; CHROMOSOME 1Q; CHROMOSOME 6Q; CHROMOSOME G BAND; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYTOGENETICS; EPENDYMOMA; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; ISOCHROMOSOME; MALE; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; PRIORITY JOURNAL; TUMOR RECURRENCE;

BRAIN NEOPLASMS; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 1; EPENDYMOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE;

EID: 0035475610     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(01)00465-4     Document Type: Article

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