Trisomies 8 and 20 in desmoid tumors

Cancer Genetics and Cytogenetics

Volumn 92, Issue 2, 1996, Pages 147-149

  Qi, Heng ^a   Cin, Paola Dal ^a   Hernândez, Jesus M ^d   Garcia, Juan Luis ^d   Sciot, Raf ^b   Fletcher, Christopher ^e   Van Eyken, Peter ^c   De Wever, Ivo ^b   Van Den Berghe, Herman ^a  

^a Center for Human Genetics   (Belgium)

^b UNIVERSITY OF LEUVEN   (Belgium)

^c DEPARTMENT OF CARDIOLOGY   (Belgium)

^d HOSPITAL UNIVERSITARIO DE SALAMANCA   (Spain)

^e BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CANCER LOCALIZATION; CELL SUSPENSION; CHILD; CHROMOSOME 20; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CLINICAL FEATURE; DESMOID TUMOR; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HISTOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; MALE; PRIORITY JOURNAL; TRISOMY; TRISOMY 8;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 20; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; FIBROMATOSIS, AGGRESSIVE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; TRISOMY;

EID: 0030455755     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(96)00170-7     Document Type: Article

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