Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
暂无分享,去创建一个
R. Weksberg | J. Squire | P. Ray | C. Shuman | M. Li | Y. Fei | A. Smith | J. Nishikawa | O. Caluseriu | J. Cameron | Adam C. Smith | C. Wei | P. Sadowski | C. Wei | L. Steele | P. Ray | I. Ambus | Madeline Li