Molecular Biology of Wilm's Tumour

نویسندگان

  • A. P. W. Shaw
  • V. Poirier
  • S. Finerty
  • P. J. Berry
  • M. G. Mott
  • N. J. Maitland
چکیده

at an early age. Furthermore, a genetic predisposition to develop the tumour is associated with aniridia, genitourinary abnormalities and mental retardation (the WAGR syndrome) (1). Children with this rare syndrome typically carry a germline deletion involving band p13 on one of the two (parentally-derived) chromosome 11 homologues (2). The inherited 11 p deletion in WAGR and hereditary Wilms' patients is thought to represent the first of two events required for initiation of Wilms'

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عنوان ژورنال:

دوره 102  شماره 

صفحات  -

تاریخ انتشار 1988