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Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome
Swati Naik, Elliott Riordan-Eva, N. Simon Thomas, Rebecca Poole, Mark Ashton, John A. Crolla, I. Karen TempleVolume:
54
Year:
2011
Language:
english
Pages:
94
DOI:
10.1016/j.ejmg.2010.09.006
File:
PDF, 616 KB
english, 2011