Detection of hyperdiploidy and chromosome breakage affecting the 1 (1cen-q12) region in lentigo malignant melanoma (LMM), superficial spreading melanoma (SSM) and congenital nevus (CN) cells in vitro by the multicolor FISH technique

Cancer Letters

Volumn 120, Issue 2, 1997, Pages 157-163

  Dopp, Elke ^a   Papp, Thilo ^a   Schiffmann, Dietmar ^a  

^a Anim Physiol Div Cell P   (Germany)

Author keywords

Chromosomal breakage; Chromosome 1; FISH; Hyperdiploidy; Melanoma

Indexed keywords

ARTICLE; CANCER GRADING; CELL CULTURE; CELL NUCLEUS; CENTROMERE; CHROMOSOME 1; CHROMOSOME BREAKAGE; CONGENITAL NEVUS; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DIPLOIDY; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROCHROMATIN; HUMAN; HUMAN CELL; INTERPHASE; MALIGNANT LENTIGO; MELANOMA; NUMERICAL CHROMOSOME ABERRATION; PRIORITY JOURNAL; STRUCTURAL CHROMOSOME ABERRATION; TETRASOMY;

ANEUPLOIDY; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 1; HUMANS; HUTCHINSON'S MELANOTIC FRECKLE; IN SITU HYBRIDIZATION, FLUORESCENCE; MELANOMA; NEVUS; SKIN NEOPLASMS; TUMOR CELLS, CULTURED;

EID: 0030663009     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3835(97)00305-4     Document Type: Article

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