Detection of molecular cytogenetic aberrations in Langerhans cell histiocytosis of bone

Human Pathology

Volumn 33, Issue 5, 2002, Pages 555-560

  Murakami, Ichiro ^a   Gogusev, Jean ^a   Fournet, Jean Christophe ^a   Glorion, Christophe ^a   Jaubert, Francis ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Comparative genomic hybridization; Langerhans cell histiocytosis; Loss of heterozygosity

Indexed keywords

ARTICLE; BONE DISEASE; CHILD; CHROMOSOME 12; CHROMOSOME 16; CHROMOSOME 17; CHROMOSOME 1P; CHROMOSOME 22Q; CHROMOSOME 2Q; CHROMOSOME 4Q; CHROMOSOME 5; CHROMOSOME 6; CHROMOSOME 7; CHROMOSOME 9; CLINICAL ARTICLE; CYTOGENETICS; DNA SEQUENCE; FEMALE; HETEROZYGOSITY LOSS; HISTIOCYTOSIS; HUMAN; HUMAN TISSUE; LANGERHANS CELL; MALE; MOLECULAR GENETICS; ONCOGENE; TUMOR SUPPRESSOR GENE;

EID: 0036305241     PISSN: 00468177     EISSN: None     Source Type: Journal    
DOI: 10.1053/hupa.2002.124035     Document Type: Article

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