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Original

PREVALENCE AND HEMATOLOGICAL CHARACTERISTICS OF β-THALASSEMIA TRAIT IN GAZIANTEP URBAN AREA, TURKEY

, MD, , MD, , MD, , MD, PhD & , MD, PhD, MPH
Pages 419-425 | Received 28 Feb 2006, Accepted 10 Mar 2006, Published online: 09 Jul 2009

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Adnan Incebiyik, Ahmet Genc, Nese Gul Hilali, Aysun Camuzcuoglu, Hakan Camuzcuoglu, Avni Kilic & Mehmet Vural. (2014) Prevalence of β-Thalassemia Trait and Abnormal Hemoglobins in Sanliurfa Province in Southeast Turkey. Hemoglobin 38:6, pages 402-404.
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Ahmet Genc, Deniz Tastemir Korkmaz, Meral Urhan Kucuk, Eyup Rencuzogullari, Selman Atakur, Suleyman Bayram, Muhittin Onderci, Tuba Koc, Sinan Aslan, Abdullah Mutalip, Muslum Faruk, Yusuf Sevgiler & Aygul Tuncdemir. (2012) Prevalence of Beta-Thalassemia Trait and Abnormal Hemoglobins in the Province of Adıyaman, Turkey. Pediatric Hematology and Oncology 29:7, pages 620-623.
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Ahmet Genc, Deniz Tastemir Korkmaz, Mehmet Buyukleyla & Murat Celiker. (2012) Prevalence and Molecular Analysis of β-Thalassemia in Adiyaman, Turkey. Hemoglobin 36:2, pages 131-138.
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Ekrem Guler, Mesut Garipardic, Tahir Dalkiran & Mehmet Davutoglu. (2010) PREMARITAL SCREENING TEST RESULTS FOR β-THALASSEMIA AND SICKLE CELL ANEMIA TRAIT IN EAST MEDITERRANEAN REGION OF TURKEY. Pediatric Hematology and Oncology 27:8, pages 608-613.
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Chutima Matayatsuk, Anne Poljak, Sonia Bustamante, George A. Smythe, Ruchaneekorn W. Kalpravidh, Pornpan Sirankapracha, Suthat Fucharoen & Prapin Wilairat. (2007) Quantitative determination of ortho- and meta-tyrosine as biomarkers of protein oxidative damage in β-thalassemia. Redox Report 12:5, pages 219-228.
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Articles from other publishers (2)

Serdar Öztuzcu, Ali Bay, Gülper Nacarkahya, Mustafa Ulaşlı, Elif Aktekin, Sinan Akbayram, Murat Korkmaz, Füsun Taşgül & Ahmet Arslan. (2016) Investigation of Distribution of Beta -Thalassemia Hereditary Mutations in Gaziantep and the Surrounding Areas. Journal of Clinical and Experimental Investigations 7:4.
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V Okan, A Cigiloglu, S Cifci, M Yilmaz & M Pehlivan. (2009) Red Cell Indices and Functions Differentiating Patients with the β-Thalassaemia Trait from those with Iron Deficiency Anaemia. Journal of International Medical Research 37:1, pages 25-30.
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