Comparative genomic hybridization detects many recurrent imbalances in central nervous system primitive neuroectodermal tumours in children

British Journal of Cancer

Volumn 79, Issue 11-12, 1999, Pages 1843-1847

  Avet Loiseau, H ^a   Venuat A M ^b   Terrier Lacombe, M J ^b   Lellouch Tubiana, A ^c   Zerah, M ^c   Vassal, G ^b  

^a INSTITUT DE BIOLOGIE   (France)

^b INSTITUT GUSTAVE ROUSSY   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

CGH; Cytogenetics; FISH; Medulloblastoma; PNET

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 10Q; CHROMOSOME 11; CHROMOSOME 12P; CHROMOSOME 17P; CHROMOSOME 17Q; CHROMOSOME 1Q; CHROMOSOME 3P; CHROMOSOME 7; CHROMOSOME 8; CHROMOSOME 9; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; HUMAN; HUMAN TISSUE; INFANT; MALE; NEUROECTODERM TUMOR; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; X CHROMOSOME;

EID: 0032970323     PISSN: 00070920     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.bjc.6690293     Document Type: Article

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