The reciprocal translocation t(9;16)(q22;p13) is a primary chromosome abnormality in basal cell carcinomas

Cancer Research

Volumn 57, Issue 3, 1997, Pages 404-406

  Jin, Yuesheng ^a,b   Mertens, Fredrik ^b   Persson, Bertil ^b   Gullestad, Hans Petter ^a   Jin, Charlotte ^b   Warloe, Trond ^a   Salemark, Lars ^b   Jonsson, Nils ^b   Risberg, Björn ^a   Mandahl, Nils ^b   Mitelman, Felix ^b   Heim, Sverre ^a,b  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BASAL CELL CARCINOMA; BASAL CELL NEVUS SYNDROME; CHROMOSOME TRANSLOCATION; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 9; CYTOGENETICS; GENE REARRANGEMENT; HUMAN; HUMAN CELL; HUMAN TISSUE; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

AGED; AGED, 80 AND OVER; CARCINOMA, BASAL CELL; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 9; HUMANS; MALE; MIDDLE AGED; TRANSLOCATION, GENETIC;

EID: 0031055867     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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