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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 1
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Original Article

Genetic studies suggest a multicentric origin for Hb G-coushatta [β22(B4)Glu→Ala]

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Pages 57-67 | Received 27 Apr 1998, Accepted 08 Aug 1998, Published online: 05 Aug 2009

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Read on this site (3)

Hafiz Al‐Nood, Saad Al‐Ismail, Lawrence King & Alison May. (2004) Prevalence of the Sickle Cell Gene in Yemen: A Pilot Study. Hemoglobin 28:4, pages 305-315.
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B. Yodsowan, J. Svasti, C. Srisomsap, P. Winichagoon & S. Fucharoen. (2000) Hb Siam [α1S(A13)Gly→Arg] is a GGT→CGT Mutation in the α1-Globin Gene. Hemoglobin 24:1, pages 71-75.
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Articles from other publishers (4)

Onur Ozturk, Sanem Arikan, Ayfer Atalay & Erol O. Atalay. (2018) Estimating the age of Hb G-Coushatta [β22(B4)Glu→Ala] mutation by haplotypes of β-globin gene cluster in Denizli, Turkey. Molecular Genetics & Genomic Medicine 6:4, pages 547-554.
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Aylin Köseler, Onur Öztürk, Ayfer Atalay & Erol Ö. Atalay. (2012) Molecular Studies on the Origin of the Hb G-Coushatta Mutation in Denizli Province of Turkey. Biochemical Genetics 51:1-2, pages 71-75.
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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 589 606 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 587 588 .

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