A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith–Wiedemann syndrome

Published 2011 View Full Article

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Title
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith–Wiedemann syndrome
Authors
Keywords
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Journal
European Journal of Medical Genetics
Volume 54, Issue 4, Pages e451-e454
Publisher
Elsevier BV
Online
2011-05-08
DOI
10.1016/j.ejmg.2011.04.009

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