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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 6
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Original Article

Prenatal Diagnosis of Sickle Cell Anemia and β-Thalassemia in Southern Turkey

M. Akif Çürük Department of Biochemistry, Medical Faculty, Çukurova University, Adana, TurkeyCorrespondence[email protected]
,
Filiz Zeren Department of Biochemistry, Medical Faculty, Çukurova University, Adana, Turkey
,
Ahmet Genç Department of Biochemistry, Medical Faculty, Çukurova University, Adana, Turkey
,
Sezen Ozavci-Aygün Department of Biochemistry, Medical Faculty, Çukurova University, Adana, Turkey
,
Yurdanur Kilinç Pediatric Haematology, Medical Faculty, Çukurova University, Adana, Turkey
&
Kiymet Aksoy Department of Biochemistry, Medical Faculty, Çukurova University, Adana, Turkey
Pages 525-530 | Received 21 Mar 2008, Accepted 23 Jun 2008, Published online: 07 Jul 2009

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Mina Ebrahimi, Javad Mohammadi-Asl & Fakher Rahim. (2021) The worldwide molecular spectrum and distribution of thalassaemia: a systematic review. Annals of Human Biology 48:4, pages 307-312.
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Azita Azarkeivan, Nader Cohan, Hamid Reza Niazkar, Arsalan Azizi & Fariba Rad. (2020) Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients . Hemoglobin 44:2, pages 109-112.
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Hossam Murad, Faten Moassas, Rami Jarjour, Yasser Mukhalalaty & Walid Al-Achkar. (2014) Prenatal Molecular Diagnosis of β-Thalassemia and Sickle Cell Anemia in the Syrian Population. Hemoglobin 38:6, pages 390-393.
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M. Sinan Beksac, Fatma Gumruk, Aytemiz Gurgey, Nur Cakar, Sezcan Mumusoglu, Ozgur Ozyuncu & Cigdem Altay. (2011) Prenatal Diagnosis of Hemoglobinopathies in Hacettepe University, Turkey. Pediatric Hematology and Oncology 28:1, pages 51-55.
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Articles from other publishers (8)

Selahaddin Tekeş, Diclehan Oral, Murat Söker, Selda Şimşek, Veysiye Hülya Uzel & Mehmet Akif Çürük. (2022) Analysis of beta globin gene mutations in Diyarbakir. Turkish Journal of Biochemistry 47:1, pages 113-118.
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Pavlos Msaouel, Priya Rao & Nizar M. Tannir. 2019. Rare Kidney Tumors. Rare Kidney Tumors 65 75 .
F. Ouali, H. Siala, A. Bibi, S. Hadj Fredj, B. Dakhlaoui, R. Othmani, F. Ouenniche, F. Zouari, B. Bouguerra, H. Rezigua, S. Fattoum & T. Messaoud. (2016) Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience. International Journal of Laboratory Hematology 38:3, pages 223-232.
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Can Boga & Hakan Ozdogu. (2016) Pregnancy and sickle cell disease: A review of the current literature. Critical Reviews in Oncology/Hematology 98, pages 364-374.
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Suheyl Asma, Ilknur Kozanoglu, Ebru Tarım, Cagla Sarıturk, Cigdem Gereklioglu, Aydan Akdeniz, Mutlu Kasar, Nurhilal H. Turgut, Mahmut Yeral, Fatih Kandemir, Can Boga & Hakan Ozdogu. (2015) Prophylactic red blood cell exchange may be beneficial in the management of sickle cell disease in pregnancy. Transfusion 55:1, pages 36-44.
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Yurdagül Erdem & Fulya Tekşen. (2013) Genetic Screening Services Provided in Turkey. Journal of Genetic Counseling 22:6, pages 858-864.
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P. C. Giordano. (2013) Strategies for basic laboratory diagnostics of the hemoglobinopathies in multi-ethnic societies: interpretation of results and pitfalls. International Journal of Laboratory Hematology 35:5, pages 465-479.
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Piero C. Giordano. (2009) Prospective and retrospective primary prevention of Hemoglobinopathies in multiethnic societies. Clinical Biochemistry 42:18, pages 1757-1766.
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