DNA copy number amplifications in human neoplasms : Review of comparative genomic hybridization studies
作者： M. Tarkkanen , A.-M. Björkqvist , S. Knuutila , V. Vidgren , O. Monni
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摘要: This review summarizes reports of recurrent DNA sequence copy number amplifications in human neoplasms detected by comparative genomic hybridization. Some the chromosomal areas with (amplicons) 1p22-p31, 1p32-p36, 1q, 2p13-p16, 2p23-p25, 2q31-q33, 3q, 5p, 6p12-pter, 7p12-p13, 7q11.2, 7q21-q22, 8p11-p12, 8q, 11q13-q14, 12p, 12q13-q21, 13q14, 13q22-qter, 14q13-q21, 15q24-qter, 17p11.2-p12, 17q12-q21, 17q22-qter, 18q, 19p13.2-pter, 19cen-q13.3, 20p11.2-p12, 20q, Xp11.2-p21, and Xp11-q13 genes therein are presented more detail. The paper than 150 references two tables can be accessed from our web site http://www.helsinki.fi/lglvwww/CMG.html. data will updated biannually until year 2001.
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