The case for newborn screening for severe combined immunodeficiency and related disorders
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.2011.06346.x/fullpdf
Reference37 articles.
1. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants;Guthrie;Pediatrics,1963
2. http://genes-r-us.uthscsa.edu/nbsdisorders.pdf
3. From developing guidelines to implementing legislation: actions of the US Advisory Committee on Heritable Disorders in Newborns and Children toward advancing and improving newborn screening;Howell;Semin Perinatol.,2010
4. Systematic evidence review of newborn screening and treatment of severe combined immunodeficiency;Lipstein;Pediatrics,2010
5. Transplantation of hematopoietic stem cells in human severe combined immunodeficiency: longterm outcomes;Buckley;Immunol. Res.,2011
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