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Hemoglobin
international journal for hemoglobin research
Volume 38, 2014 - Issue 6
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Research Article

Prevalence of β-Thalassemia Trait and Abnormal Hemoglobins in Sanliurfa Province in Southeast Turkey

Adnan IncebiyikDepartment of Obstetrics and GynaecologyHarran University, School of Medicine SanliurfaTurkeyCorrespondence[email protected]
,
Ahmet GencAdıyaman Univesity, Vocational School of Health Services AdiyamanTurkey
,
Nese Gul HilaliDepartment of Obstetrics and GynaecologyHarran University, School of Medicine SanliurfaTurkey
,
Aysun CamuzcuogluDepartment of Obstetrics and GynaecologyHarran University, School of Medicine SanliurfaTurkey
,
Hakan CamuzcuogluDepartment of Obstetrics and GynaecologyHarran University, School of Medicine SanliurfaTurkey
,
Avni KilicDepartment of Obstetrics and GynaecologyHarran University, School of Medicine SanliurfaTurkey
&
Mehmet VuralDepartment of Obstetrics and Gynaecology, Marmara University, School of Medicine IstanbulTurkey
 show all
Pages 402-404 | Received 24 Apr 2014, Accepted 22 May 2014, Published online: 18 Nov 2014

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Read on this site (1)

Duran Canatan & Serpil Delibas. (2016) Report on Ten Years’ Experience of Premarital Hemoglobinopathy Screening at a Center in Antalya, Southern Turkey. Hemoglobin 40:4, pages 273-276.
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Articles from other publishers (3)

Ahmet Kursad Gunes & Hilmi Erdem Gozden. (2021) The Spectrum of Beta-Thalassemia Mutations in Syrian Refugees and Turkish Citizens. Cureus.
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Eman S. Alsaeed, Ghada N. Farhat, Abdullah M. Assiri, Ziad Memish, Elawad M. Ahmed, Mohammad Y. Saeedi, Mishal F. Al-Dossary & Hisham Bashawri. (2017) Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program, 2011–2015. Journal of Epidemiology and Global Health 7:S1, pages S41.
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Ahmet Uçar, Nergiz Öner, Gülcihan Özek, Mehmet Güli Çetinçakmak, Mahmut Abuhandan, Ali Yıldırım, Cemil Kaya, Sena Ünverdi, Hamdi Cihan Emeksiz, Yasin Yılmaz & Aylin Yetim. (2016) Evaluation of the glucocorticoid, mineralocorticoid, and adrenal androgen secretion dynamics in a large cohort of patients aged 6–18 years with transfusion-dependent β-thalassemia major, with an emphasis on the impact of cardiac iron load. Endocrine 53:1, pages 240-248.
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