Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney

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Title: Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney
Authors: Haruta, Masayuki, Arai, Yasuhito, Okita, Hajime, Tanaka, Yukichi, Takimoto, Tetsuya, Kamijo, Takehiko, Oue, Takaharu, Souzaki, Ryota, Taguchi, Tomoaki, Kuwahara, Yasumichi, Chin, Motoaki, Nakadate, Hisaya, Hiyama, Eiso, Ishida, Yasushi, Koshinaga, Tsugumichi, Kaneko, Yasuhiko
Source: Genes, chromosomes & cancer. 60(8):546-558
Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122686364.0x000001&indx=1&recIds=ETOCvdc_100122686364.0x000001
Database: British Library Document Supply Centre Inside Serials & Conference Proceedings
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ISSN:10452257
Published in:Genes, chromosomes & cancer
Language:English