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                                       Details for article 28 of 32 found articles
 
 
  Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol
 
 
Title: Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol
Author: Lobitz, Stephan
Frömmel, Claudia
Brose, Annemarie
Blankenstein, Oliver
Turner, Charles
Dalton, R. Neil
Daniel, Yvonne
Klein, Jeannette
Appeared in: Annals of hematology
Paging: Volume 101 () nr. 8 pages 1859-1860
Year: 2022-03-16
Contents:
Publisher: Springer Berlin Heidelberg, Berlin/Heidelberg
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 28 of 32 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands