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10. [Molecular diagnosis in a Korean family with thalassemia intermedia due to co-inheritance of triplicated alpha-globin genes (alphaalpha/alphaalphaalpha(anti 3.7)) and beta-thalassemia trait (IVS-II-1 G-->A)]. Chen M; Han JY; Sun Q; Kim IH; Ren Z; Huang S; Zeng Y Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):195-7. PubMed ID: 11876981 [TBL] [Abstract][Full Text] [Related]
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12. Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes. Mehta PR; Upadhye DS; Sawant PM; Gorivale MS; Nadkarni AH; Shanmukhaiah C; Ghosh K; Colah RB Ann Hematol; 2015 Dec; 94(12):1953-8. PubMed ID: 26319530 [TBL] [Abstract][Full Text] [Related]
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16. Prevalence of beta-thalassemia trait and glucose-6-phosphate dehydrogenase deficiency in Iranian Jews. Karimi M; Yavarian M; Afrasiabi A; Dehbozorgian J; Rachmilewitz E Arch Med Res; 2008 Feb; 39(2):212-4. PubMed ID: 18164966 [TBL] [Abstract][Full Text] [Related]
17. Detection of a rare mutation in an Iranian family: codons 37/38/39 (7 bp deletion). Zadeh-Vakili A; Eshghi P Hemoglobin; 2009; 33(6):523-7. PubMed ID: 19958201 [TBL] [Abstract][Full Text] [Related]
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