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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 1
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Letter to the Editor

A Further Note on the Thalassemia Screening Program in the Muğla Region of Turkey

References

  • Topal Y, Topal H, Ceyhan MN, et al. The prevalence of hemoglobinopathies in young adolescents in the Province of Muğla in Turkey: Results of a screening program. Hemoglobin. 2015;39(4):247–250
  • Arcasoy A, Turan F, Yeşil N, et al. Muğla ili ve çevresinde thalassemia ve anormal hemoglobin sıklığının taranması. Pediatride Yönelişler. 1994;1(1):78–80
  • Özdemir S, Timur İH, Gencer İ, et al. Premarital screening in Muğla region of Turkey. Turk J Hematol. 2009;26(4):214–215
  • Yenice Ş, Kemahlı S, Bilenoğlu O, et al. Two rare hemoglobin variants in the Turkish population (Hb G-Coushatta (β22(B4)Glu → Ala) and Hb J-Iran (β77(EF1)His → Asp). Turk J Hematol. 2000;17(1):27–28
  • Akar E, Ozdemir S, Hakki Timur I, Akar N. First observation of homozygous Hemoglobin Hamadan [β56(D7)Gly → Arg] and β thalassemia (-29 G > A)-Hemoglobin Hamadan combination in a Turkish family. Am J Hematol. 2003;74(4):280–282
  • Akar N, Akar E, Özdemir S. A further case of Hb J-Iran (β77(EF1)His → Asp) in Muğla, Turkey. Turk J Hematol. 2007;24(1):37–38

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