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Nature Genetics  20, 66 - 69 (1998)
doi:10.1038/1727

Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas

Zhengping Zhuang, Won-Sang Park, Svetlana Pack, Laura Schmidt, Alexander O. Vortmeyer, Evgenia Pak, Thu Pham, Robert J. Weil, Sonja Candidus, Irina A. Lubensky, W. Marston Linehan, Berton Zbar & Gregor Weirich
 
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Figure 1. FISH analysis of lymphoblastoid cell line and tumour tissues from HPRC patients.
a, Two colour FISH of metaphase chromosomes prepared from lymphoblastoid cell cultures obtained from patient 2. Cosmid clone c182b3, which contains the MET gene (rhodamine, red signal) and a centromeric alpha-satellite probe (FITC, green signal) specific for chromosome 7 as a reference marker. b, Interphase FISH on tumour touch preparation showing the three copies of MET (rhodamine, red signal), using c182b3 combined with a centromeric alpha-satellite probe (FITC, green signal) specific for chromosome 17. c, Two colour FISH of metaphase chromosomes from patient 2, as above, using a chromosome 7-specific painting probe, which shows the two germline copies. d, Interphase FISH showing three copies of chromosome 7 in one of the tumours using the chromosome 7-specific painting probe (rhodamine, red signal) and the chromosome 7 alpha-satellite probe (FITC, green signal).

 
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