Monosomy 9q and trisomy 16q in a case of congenital solitary infantile myofibromatosis

Virchows Archiv

Volumn 445, Issue 5, 2004, Pages 537-540

  Sirvent, Nicolas ^a   Perrin, Christophe ^a   Lacour, Jean Philippe ^a   Maire, Georges ^b   Attias, Rita ^b   Pedeutour, Florence ^b  

^a UNIVERSITY HOSPITAL OF NICE   (France)

^b CENTRE HOSPITALIER UNIVERSITAIRE DE NICE   (France)

Author keywords

Children; Cytogenetics; FISH; Infantile myofibromatosis; Soft tissue neoplasms; Translocation

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 16; CHROMOSOME 9; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HISTOPATHOLOGY; HUMAN; IMMUNOHISTOCHEMISTRY; LEIOMYOMA; MONOSOMY; MONOSOMY 9Q; PRESCHOOL CHILD; PRIORITY JOURNAL; SOLITARY INFANTILE MYOFIBROMATOSIS; TRISOMY 16; TRISOMY 16Q;

ADULT; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; MONOSOMY; MYOFIBROMATOSIS; SOFT TISSUE NEOPLASMS; TRISOMY;

EID: 9944225234     PISSN: 09456317     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00428-004-1097-y     Document Type: Article

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