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                                       Details for article 12 of 22 found articles
 
 
  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
 
 
Title: 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
Author: Naik, Swati
Riordan-Eva, Elliott
Thomas, N. Simon
Poole, Rebecca
Ashton, Mark
Crolla, John A.
Temple, I. Karen
Appeared in: European journal of medical genetics
Paging: Volume 54 (2011) nr. 1 pages 5 p.
Year: 2011
Contents:
Publisher: Elsevier Masson SAS
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 12 of 22 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands