Comprehensive characterization of Alu-mediated breakpoints in germline VHL gene deletions and rearrangements in patients from 71 VHL families

Vocke, CD; Ricketts, CJ; Schmidt, LS; Ball, MW; Middelton, LA; Zbar, B; Linehan, WM

Linehan, WM (corresponding author), NCI, Urol Oncol Branch, Bldg 10 CRC Room 1-5940, Bethesda, MD 20892 USA.

HUMAN MUTATION, ; ():

Abstract

Von Hippel-Lindau (VHL) is a hereditary multisystem disorder caused by germline alterations in the VHL gene. VHL patients are at risk for benign as we......

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