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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 1
134
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Short Communication

Further Identification of Hb G-Coushatta [β22(B4)Glu→Ala (GAA→GCA)] in Thailand by the Polymerase Chain Reaction-Single-Strand Conformation Polymorphism Technique and by Amplification Refractory Mutation System-Polymerase Chain Reaction

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Pages 93-99 | Received 24 Aug 2005, Accepted 29 Aug 2006, Published online: 07 Jul 2009

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Narges Soozangar, Ehsan Abbaspour, Haleh Mokaber, Zahra Nematollahi & Behzad Davarnia. (2023) A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran. Human Genome Variation 10:1.
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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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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 .
Cameron Mroske, John Muci, Jicheng Wang, Kai Li, Wenjia Song, Jin Yan, Jinong Feng, Qiang Liu & Steve S. Sommer. (2007) Toward a fluorescent single-strand conformation polymorphism technique that detects all mutations: F-DOVAM-S. Analytical Biochemistry 368:2, pages 250-257.
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