Newborn Screening for Hemoglobinopathies Using Capillary Electrophoresis
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Publisher
Humana Press
Link
http://link.springer.com/content/pdf/10.1007/978-1-62703-029-8_13.pdf
Reference20 articles.
1. Bunn AF, Forget BG, Ranney HM (1977) Human hemoglobins. W.B. Saunders, Philadelphia
2. van den Berg HM et al (1999) Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl. Hemoglobin 23:135–144
3. Weatherall DJ, Clegg JB (2001) The thalassaemia syndromes, 4th edn. Wiley-Blackwell, Oxford
4. Harteveld CL et al (2003) Novel 112 kb (epsilonGgammaAgamma) deltabeta-thalassaemia deletion in a Dutch family. Br J Haematol 122:855–858
5. Harteveld CL et al (2008) Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients. Blood Cells Mol Dis 40:312–316
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