Screening for glucose-6-phosphate dehydrogenase deficiency in neonates: a comparison between cord and peripheral blood samples
Author:
Funder
King Abdullah International Medical Research Center
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1186/s12887-017-0912-y.pdf
Reference17 articles.
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2. Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group. Bull World Health Organ. 1989;6796:601–11.
3. Kaplan M, Hammerman C. Glucose-6-phosphate dehydrogenase deficiency and severe neonatal hyperbilirubinemia: a complexity of interactions between genes and environment. Semin Fetal Neonatal Med. 2010;15:148–56.
4. Kosaryan M, Mahdavi MR, Jalali H, Roshan P. Why does the Iranian national program of screening newborns for G6PD enzyme deficiency miss a large number of affected infants? Pediatr Hematol Oncol. 2014 Feb;31(1):95–100.
5. As W, El-Hazmi MA. G6PD deficiency, distribution and variants in Saudi Arabia: an overview. Ann Saudi Med. 2001;21:174–7.
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