Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice
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DOI: 10.3390/cancers14133083
Abstract: Simple Summary Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is an inborn overgrowth disorder caused by molecular alterations in chromosome 11p15.5. These molecular changes affect so-called imprinted genes, i.e., genes which underlie a complex regulation which is… read more here.
Keywords: bwsp; wiedemann syndrome; spectrum; beckwith wiedemann ... See more keywords