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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 2
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Short Communications

βS-Globin Gene Cluster Haplotypes in the West Bank of Palestine

Fekri Samarah Department of Biochemistry, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece
,
Suhail Ayesh Molecular Genetics Laboratory, Makassed Islamic Charitable Hospital, Jerusalem, Israel
,
Miranda Athanasiou First Paediatric Clinic, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece
,
John Christakis Department of Haematology, Theagenion Cancer Centre, Thessaloniki, Greece
&
Norma Vavatsi Department of Biochemistry, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, GreeceCorrespondence[email protected]
Pages 143-149 | Received 08 Apr 2008, Accepted 19 Jan 2009, Published online: 07 Jul 2009

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Heba H. Abou-Elew, Ilham Youssry, Shireen Hefny, Rania H. Hashem, Nevine Fouad & Rania A. Zayed. (2018) βS globin gene haplotype and the stroke risk among Egyptian children with sickle cell disease. Hematology 23:6, pages 362-367.
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Nasir A.S. Al-Allawi, Sana D. Jalal, Farida F. Nerwey, Galawezh O.O. Al-Sayan, Sahima S.M. Al-Zebari, Awny A. Alshingaly, Raji D. Markous, Jaladet M.S. Jubrael & Hanan Hamamy. (2012) Sickle Cell Disease in the Kurdish Population of Northern Iraq. Hemoglobin 36:4, pages 333-342.
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Articles from other publishers (10)

Abozer Y. Elderdery, Abdullah Alsrhani, Badr Alzahrani, Muhammad Atif, Ahmed I. Refaiy, Hussain Shiwani, Amin Abbas & Dawelbiet A. Yahia. (2022) Molecular Analysis of Xmn1-Polymorphic Site ´5 to Gγ of the β-Globin Gene Cluster in a Saudi Population of Jazan Region in Correlation with Hb F Expression. Evidence-Based Complementary and Alternative Medicine 2022, pages 1-6.
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Fekri Samarah, Mahmoud A. Srour & Kamal Dumaidi. (2021) Plasma Lipids and Lipoproteins in Sickle Cell Disease Patients in the Northern West Bank, Palestine. BioMed Research International 2021, pages 1-8.
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Fekri Samarah & Mahmoud A. Srour. (2018) Factor V Leiden G1691A and prothrombin G20210A mutations among Palestinian patients with sickle cell disease. BMC Hematology 18:1.
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Fekri Samarah, Mahmoud A. Srour, Dirgham Yaseen & Kamal Dumaidi. (2018) Frequency of Red Blood Cell Alloimmunization in Patients with Sickle Cell Disease in Palestine. Advances in Hematology 2018, pages 1-7.
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Kaveh Jaseb, Abolfazl Ramezani, Mohammad Ali Jalali Far, Javad Mohammadi-Asl, Abbas Khosravi & Najmaldin Saki. (2017) Association between beta globin haplotypes, HBBP1 and HMOX1 polymorphisms in relation to HbF among sickle cell anemia patients: a study in Southwest Iran. Comparative Clinical Pathology 26:5, pages 1149-1155.
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Juliana D. Lindenau, Sandrine C. Wagner, Simone M. de Castro & Mara H. Hutz. (2016) The effects of old and recent migration waves in the distribution of HBB*S globin gene haplotypes. Genetics and Molecular Biology 39:4, pages 515-523.
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Valentina J. Ngo BitounguiGift D. PuleNeil HanchardJeanne NgogangAmbroise Wonkam. (2015) Beta-Globin Gene Haplotypes Among Cameroonians and Review of the Global Distribution: Is There a Case for a Single Sickle Mutation Origin in Africa?. OMICS: A Journal of Integrative Biology 19:3, pages 171-179.
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Hanan A. Hamamy & Nasir A. S. Al-Allawi. (2012) Epidemiological profile of common haemoglobinopathies in Arab countries. Journal of Community Genetics 4:2, pages 147-167.
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A. Y. ELDERDERY, J. MILLS, B. A. MOHAMED, A. J. COOPER, A. O. MOHAMMED, N. ELTIEB & J. OLD. (2012) Molecular analysis of the β-globin gene cluster haplotypes in a Sudanese population with sickle cell anaemia. International Journal of Laboratory Hematology 34:3, pages 262-266.
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Turker Bilgen, Yunus Arikan, Duran Canatan, Akif Yeşilipek & Ibrahim Keser. (2011) The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population. Blood Cells, Molecules, and Diseases 46:3, pages 226-229.
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