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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 4
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Original Article

Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation

Ferda OzkinayDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, TurkeyCorrespondence[email protected]
,
Huseyin OnayDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
,
Emin KaracaDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
,
Esra ArslanDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
,
Biray ErturkDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
,
Asli Ece SolmazDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
,
Ismihan Merve TekinDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
,
Ozgur CoguluDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
,
Yeşim AydinokDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
&
Canan VerginDepartment of Medical Genetics, Ege University Faculty of Medicine, Medical School Hospital, Bornova, Izmir, Turkey
 show all
Pages 230-234 | Received 08 Aug 2014, Accepted 06 Oct 2014, Published online: 15 Jun 2015

Citations (8)

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Read on this site (3)

Sedat Yılmaz. (2019) The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey. Hemoglobin 43:3, pages 174-181.
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Abdul Aziz, Sudipta A. Das, Waqar A. Khan, Salma Sadiya, Bilquis Banu, Golam Sarwardi & Rowshon Z. Luna. (2017) A Novel β-Thalassemia Insertion/Frameshift Mutation Between Codons 77/78 (p.Leu78Profs*13 or HBB: c.235_236insC) Observed in a Family in Bangladesh. Hemoglobin 41:4-6, pages 311-313.
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Sheng He, Li Lin, Yuan Wei, Biyan Chen, Shang Yi, Qiuli Chen, XiaoXia Qiu, Hongwei Wei, Guojian Li & Chenguang Zheng. (2016) Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family. Hemoglobin 40:4, pages 277-279.
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Articles from other publishers (5)

Abdullah Arpaci, Bahar Unlu Gul, Oguzhan Ozcan, Gul Ilhan, Cigdem El, Emre Dirican, Sibel Elmacioglu & Hasan Kaya. (2021) Presentation of two new mutations in the 3′untranslated region of the β-globin gene and evaluating the molecular spectrum of thalassemia mutations in the Mediterranean region of Turkey. Annals of Hematology 100:6, pages 1429-1438.
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Ebru Yilmaz Keskin, Öznur Acar & Halil Özbas. (2021) Missed Diagnosis of β-Thalassemia Trait in Premarital Screening Due to Accompanying HbA2-Yialousa (HBD: c.82G>T). Journal of Pediatric Hematology/Oncology 43:1, pages e103-e104.
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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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Chi-Kong Li. (2017) New trend in the epidemiology of thalassaemia. Best Practice & Research Clinical Obstetrics & Gynaecology 39, pages 16-26.
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A Uludağ, A Uysal, A Uludağ, YH Ertekin, M Tekin, B Kütük, F Silan & Ö Özdemir. (2016) Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey. Balkan Journal of Medical Genetics 19:1, pages 29-34.
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