Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Link
http://www.nature.com/articles/jp2009136.pdf
Reference16 articles.
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2. Maisels MJ, Kring E . The contribution of hemolysis to early jaundice in normal newborns. Pediatrics 2006; 118 (1): 276–279.
3. Porter ML, Dennis BL . Hyperbilirubinemia in the term newborn. Am Fam Physician 2002; 65 (4): 599–606.
4. Dobrowolski SF, Banas RA, Suzow JG, Berkley M, Naylor EW . Analysis of common mutations in the galactose-1-phosphate uridyl transferase gene: new assays to increase the sensitivity and specificity of newborn screening for galactosemia. J Mol Diagn 2003; 5 (1): 42–47.
5. Kaye CI, Accurso F, La Franchi S, Lane PA, Hope N, Sonya P et al. Newborn screening fact sheets. Pediatrics 2006; 118 (3): e934–e963.
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