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Hemoglobin
international journal for hemoglobin research
Volume 9, 1985 - Issue 2
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Original Article

Compound Heterozygosity for two Genotypes of α-Thalassemia-2 : Hematological, Biosynthetic and DNA Studies

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Pages 111-126 | Received 22 Oct 1984, Accepted 14 Feb 1985, Published online: 07 Jul 2009

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Read on this site (3)

W. A. Schroeder, Darleen R. Powars, Lois M. Kay, Linda S. Chan, Van Huynh, Joan B. Shelton & J. Roger Shelton. (1989) β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California. Hemoglobin 13:4, pages 325-353.
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C. C. Thompson, M. A. M. Ali, M. Vacovsky & S. Boyadjian. (1989) The Interaction of Anti 3. 7 Type Quadruplicated α-Globin Genes and Heterozygous β-Thalassemia. Hemoglobin 13:2, pages 125-135.
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S. H. Embury. (1988) The Different Types of α-Thalassemia-2: Genetic Aspects. Hemoglobin 12:5-6, pages 445-453.
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Articles from other publishers (2)

S. Safaya, P. Mullaney & R. F. Rieder. (1987) Dysfunctional α-globin genes in hemoglobin H disease in blacks: Variation in restriction fragment size permits the detection of the -α/-αT genotype. American Journal of Hematology 26:4, pages 329-339.
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David H.K. Chui, Shiu C. Wong, Siu-Wah Chung, Margaret Patterson, Sunita Bhargava & Man-Chiu Poon. (1986) Embryonic ζ-Globin Chains in Adults: a Marker for α-Thalassemia-1 Haplotype Due to a >17.5-kb Deletion. New England Journal of Medicine 314:2, pages 76-79.
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