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Original Article

Hemoglobinopathies in the District of Antalya, Turkey

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Pages 289-291 | Received 12 Aug 1992, Accepted 06 Nov 1992, Published online: 09 Jul 2009

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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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Andreani R. Kyrri, Xenia Felekis, Eleni Kalogerou, Barbara J. Wild, Loukas Kythreotis, Marios Phylactides & Marina Kleanthous. (2009) Hemoglobin Variants in Cyprus. Hemoglobin 33:2, pages 81-94.
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Erol Ö. Atalay, Ayfer Atalay, Emre Üstel, Sanem Yildiz, Onur Öztürk, Aylin Köseler & Anzel Bahadir. (2007) Genetic Origin of Hb D-Los Angeles [β121(GH4)Glu→Gln, GAA→CAA] According to the β-Globin Gene Cluster Haplotypes. Hemoglobin 31:3, pages 387-391.
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Erol Ö. Atalay, Hasan Koyuncu, Berna Turgut, Ayfer Atalay, Sanem Yildiz, Anzel Bahadir & Aylin Köseler. (2005) High Incidence of Hb D-Los Angeles [β121(GH4)Glu→Gln] in Denizli Province, Aegean Region of Turkey. Hemoglobin 29:4, pages 307-310.
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Ghazi O. Tadmouri & A. Nazlı Başak. (2001) β-THALASSEMIA IN TURKEY: A REVIEW OF THE CLINICAL, EPIDEMIOLOGICAL, MOLECULAR, AND EVOLUTIONARY ASPECTS. Hemoglobin 25:2, pages 227-239.
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Esra FIRAT OĞUZ & Funda EREN. (2022) THE EVALUATION OF TERTIARY CARE CENTER HEMOGLOBIN VARIANT DATA FOR THREE YEARS PERIODÜçüncü Basamak Sağlık Merkezi Hemoglobin Varyant Verilerinin Üç Yıllık Değerlendirilmesi. Kırıkkale Üniversitesi Tıp Fakültesi Dergisi 24:3, pages 505-509.
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Hayat Alafari & Faris Q. Alenzi. (2020) Biochemical and molecular analysis of the beta-globin gene and LCR region on Saudi β-thalassemia patients. Saudi Journal of Biological Sciences 27:11, pages 3106-3112.
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Sinem YALÇINTEPE. (2019) Trakya Üniversitesi Tıp Fakültesi Genetik Hastalıklar Tanı Merkezinde beta talasemi minor kliniği ile incelenen bireylerde görülen beta globin mutasyonları ve sıklığıBeta globin mutations in beta thalassemia minor patients in Genetics Diagnosis Center of Trakya University Faculty of Medicine. Ege Tıp Dergisi 58:4, pages 330-335.
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Sanjay Pandey, Rahasya Mani Mishra, Sweta Pandey, Vineet Shah & Renu Saxena. (2012) Molecular characterization of hemoglobin D Punjab traits and clinical-hematological profile of the patients. Sao Paulo Medical Journal 130:4, pages 248-251.
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N. NAL, A. E. MANGUOGLU, C. F. SARGIN, I. KESER, A. KUPESIZ, A. YESILIPEK & G. LULECI. (2005) Two rare mutations in Turkey: IVS I.130(G-C) and IVS II.848(C-A). Clinical and Laboratory Haematology 27:4, pages 274-277.
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MA Yesilipek, V Hazar, A Küpesiz, A Kızılörs, A Uguz & O Yegin. (2001) Peripheral blood stem cell transplantation in children with beta-thalassemia. Bone Marrow Transplantation 28:11, pages 1037-1040.
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S Menon & D A Isenberg. (1995) Rheumatological manifestations of haematological diseases.. Annals of the Rheumatic Diseases 54:10, pages 787-795.
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