Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization

Genes Chromosomes and Cancer

Volumn 43, Issue 3, 2005, Pages 294-301

  Zielinski, Boris ^a   Gratias, Sandrine ^b   Toedt, Grischa ^a   Mendrzyk, Frank ^a   Stange, Daniel E ^a   Radlwimmer, Bernhard ^a   Lohmann, Dietmar R ^b   Lichter, Peter ^a  

^a GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^b UNIVERSITY OF DUISBURG ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT;

ARTICLE; CHROMOSOME 16Q; CHROMOSOME 19Q; CHROMOSOME 1Q; CHROMOSOME 2P; CHROMOSOME 6P; CHROMOSOME ARM; CHROMOSOME BAND; CHROMOSOME LOSS; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENE DELETION; GENE MUTATION; HUMAN; HUMAN CELL; MALE; PRIORITY JOURNAL; RB1 GENE; RETINOBLASTOMA;

ALLELIC IMBALANCE; CELL LINE, TUMOR; CHROMOSOME ABERRATIONS; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, BACTERIAL; EYE NEOPLASMS; GENE AMPLIFICATION; HUMANS; IN SITU HYBRIDIZATION; NUCLEIC ACID HYBRIDIZATION; RETINOBLASTOMA; SEQUENCE DELETION;

EID: 19444377455     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/gcc.20186     Document Type: Article

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