Trisomy 7 and 17 mark papillary renal cell tumours irrespectively of variation of the phenotype.

@article{Blint2009Trisomy7A,
  title={Trisomy 7 and 17 mark papillary renal cell tumours irrespectively of variation of the phenotype.},
  author={Ildik{\'o} B{\'a}lint and Adrianna Szponar and Anna Jauch and Gyula Kov{\'a}cs},
  journal={Journal of clinical pathology},
  year={2009},
  volume={62 10},
  pages={892-5}
}
BACKGROUND Papillary renal cell tumours (RCTs) have been described as a genetic entity. Recently, papillary RCTs have been divided into small (type 1) and large (type 2) cell tumours. Subsequent DNA analyses have resulted in controversial data regarding putative genetic changes marking type 1 and type 2 tumours. AIM The aim of this study was to improve the original description that papillary RCT is a genetic entity regardless of the phenotypic variation. METHODS DNA from 163 papillary RCTs… CONTINUE READING

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