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                                       Details for article 5 of 22 found articles
 
 
  A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period
 
 
Title: A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period
Author: Gundel, Florian
Eber, Stefan
Heep, Axel
Appeared in: Annals of hematology
Paging: Volume 90 (2010) nr. 2 pages 231-232
Year: 2010
Contents:
Publisher: Springer-Verlag, Berlin/Heidelberg
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 5 of 22 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands