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                                       Details for article 19 of 26 found articles
 
 
  1.4Mb recurrent 22q11.2 distal deletion syndrome, two new cases expand the phenotype
 
 
Title: 1.4Mb recurrent 22q11.2 distal deletion syndrome, two new cases expand the phenotype
Author: Rødningen, Olaug K.
Prescott, Trine
Eriksson, Ann-Sofie
Røsby, Oddveig
Appeared in: European journal of medical genetics
Paging: Volume 51 (2008) nr. 6 pages 5 p.
Year: 2008
Contents:
Publisher: Elsevier Masson SAS
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 19 of 26 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands