Genetic Predisposition to β-Thalassemia and Sickle Cell Anemia in Turkey: A Molecular Diagnostic Approach
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Publisher
Humana Press
Link
http://link.springer.com/content/pdf/10.1007/978-1-61737-954-3_19
Reference84 articles.
1. Weatherall D (1994) The thalassemias. WB Saunders, Philadelphia
2. Tuzmen S, Schechter AN (2001) Genetic diseases of hemoglobin: diagnostic methods for elucidating beta-thalassemia mutations. Blood Rev 15:19–29
3. Flint J, Harding RM, Boyce AJ, Clegg JB (1998) The population genetics of the haemoglobinopathies. Baillières Clin Haematol 11:1–51
4. Weatherall DJ, Miller LH, Baruch DI, Marsh K, Doumbo OK, Casals-Pascual C, Roberts DJ (2002) Malaria and the red cell. Hematology Am Soc Hematol Educ Program 2002(1):35–57
5. Basak AN (2007) The molecular pathology of beta-thalassemia in Turkey: the Bogazici university experience. Hemoglobin 31:233–241
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Identification of β-globin haplotypes linked to sickle hemoglobin (Hb S) alleles in Mazandaran province, Iran;Genes & Genetic Systems;2016
2. Hypermethylation of IGSF4 gene for noninvasive prenatal diagnosis of thalassemia;Medical Science Monitor;2012
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