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                                       Details for article 206 of 218 found articles
 
 
  The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening
 
 
Title: The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening
Author: Georgiou, Theodoros
Ho, Gladys
Vogazianos, Marios
Dionysiou, Maria
Nicolaou, Alexia
Chappa, Georgia
Nicolaides, Paola
Stylianidou, Goula
Christodoulou, John
Drousiotou, Anthi
Appeared in: Clinical biochemistry
Paging: Volume 45 (2012) nr. 7-8 pages 5 p.
Year: 2012
Contents:
Publisher: The Canadian Society of Clinical Chemists
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 206 of 218 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands