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Hemoglobin
international journal for hemoglobin research
Volume 21, 1997 - Issue 3
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Original Article

Historical and Anthropological Correlates of βS Haplotypes and α- and β-Thalassemia Alleles in the Arabian Peninsula

A. D. Adekile Department of Paediatrics Faculty of Medicine, Kuwait University, Safat, 131 10, Kuwait
Pages 281-296 | Received 21 Jun 1996, Accepted 27 Jan 1997, Published online: 07 Jul 2009

Citations (13)

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Slaheddine Fattoum, Taeib Messaoud & Amina Bibi. (2004) Molecular Basis of β‐Thalassemia in the Population of Tunisia. Hemoglobin 28:3, pages 177-187.
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Ajit C. Gorakshakar, Supriya P. Phanasgaonkar, Anita H. Nadkarni, Roshan B. Colah & Dipika Mohanty. (2004) Detection of Rare β‐Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians. Hemoglobin 28:1, pages 15-24.
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Articles from other publishers (11)

Mona El-Ghamrawy, Marianne E. Yassa, Angie M. S. Tousson, Marwa Abd El-hady, Erini Mikhaeil, Nada B. Mohamed & Mervat Mamdooh Khorshied. (2020) Association between BCL11A, HSB1L-MYB, and XmnI γG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients. Annals of Hematology 99:10, pages 2279-2288.
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Pacint Moez, Reham Moftah & Hayam A. Mahmoud. (2018) A study on the genotype frequency of $$-158~\hbox {G}\gamma $$ - 158 G γ ( $$\hbox {C}{\rightarrow }\hbox {T}$$ C → T ) Xmn1 polymorphism in a sickle cell trait cohort from Siwa Oasis, Egypt. Journal of Genetics 97:2, pages 505-511.
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Adekunle Adekile & Julie Makani. 2016. Sickle Cell Anemia. Sickle Cell Anemia 339 370 .
Aparna A. Bhanushali, P.K. Patra, D. Nair, H. Verma & B.R. Das. (2015) Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients. Blood Cells, Molecules, and Diseases 54:1, pages 4-8.
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Idowu AkinsheyeAbdulrahman Alsultan, Nadia Solovieff, Duyen NgoClinton T. BaldwinPaola Sebastiani, David H. K. ChuiMartin H. Steinberg. (2011) Fetal hemoglobin in sickle cell anemia. Blood 118:1, pages 19-27.
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Zakaria Mohammad Al Hawsawi, Mona Hamza Sairafy, Ahmed Mohamed Tarawah, Mohammed Adnan Zolaly & Abdul Rahman Soad Al Hegaily. (2010) Experience with Combination Therapy of Deferiprone and Desferrioxamine in β-Thalassemia Major Patients with Iron Overload at Maternity and Children Hospital, Al Madinah Al Munawarah, Saudi Arabia. Journal of Taibah University Medical Sciences 5:1, pages 27-35.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg & Ronald L. Nagel. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 638 657 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 623 624 .
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Shahina Daar, H. Mohamed Hussain, David Gravell, Ronald L. Nagel & Rajagopal Krishnamoorthy. (2000) Genetic epidemiology of HbS in Oman: Multicentric origin for the β S gene . American Journal of Hematology 64:1, pages 39-46.
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Oswaldo Castro. (2002) MANAGEMENT OF SICKLE CELL DISEASE: RECENT ADVANCES AND CONTROVERSIES. British Journal of Haematology 107:1, pages 2-11.
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