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Newborn screening for primary immunodeficiencies: beyond SCID and XLA

  • Published:2011-12 Issue:1 Volume:1246 Page:118-130
  • ISSN:0077-8923
  • Container-title:Annals of the New York Academy of Sciences
  • language:en
  • Short-container-title:

Author:

Borte Stephan,Wang Ning,Óskarsdóttir Sólveig,von Döbeln Ulrika,Hammarström Lennart

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Reference130 articles.

1. Newborn screening for genetic disorders;Fernhoff;Pediatr. Clin. North Am.,2009

2. Development of population-based newborn screening for severe combined immunodeficiency;Chan;J. Allergy Clin. Immunol.,2005

3. Primary immunodeficiency disorders in Sweden: cases among children, 1974-1979;Fasth;J. Clin. Immunol.,1982

4. Primary immunodeficiency diseases in Singapore-the last 11 years;Lim;Singapore Med. J.,2003

5. Incidence and temporal trends of primary immunodeficiency: a population-based cohort study;Joshi;Mayo Clin. Proc.,2009
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