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Hemoglobin
international journal for hemoglobin research
Volume 5, 1981 - Issue 5
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Original Article

The Frequency of the AγT Gene in the Presence and Absence of the βs or βC Gene in the Black Poplilation of the Southeastern USA

T. H. J. Huisman Laboratory of Protein Chemistry Comprehensive Sickle Cell Center, Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912, USA
&
B. Webber Laboratory of Protein Chemistry Comprehensive Sickle Cell Center, Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912, USA
Pages 441-451 | Received 15 Apr 1981, Accepted 13 May 1981, Published online: 07 Jul 2009

Citations (4)

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Read on this site (2)

Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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T. Harano & T. H. J. Huisman. (1984) Hemoglobin Abnormalities in a Black Family with Hb S, Hereditary Persistence of HB F, and A γ Chain Variant; a Reevaluation Through Gene Mapping. Hemoglobin 8:6, pages 549-568.
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Articles from other publishers (2)

M.E. Headlee, M.B. Gardiner, A.L. Reese & T.H.J. Huisman. (1983) The distribution of fetal hemoglobin and the types of γ chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies. Biochemical Medicine 29:3, pages 337-354.
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T. H. J. Huisman, A. L. Reese, M. B. Gardiner, J. B. Wilson, H. Lam, A. Reynolds, S. Nagle, P. Trowell, Zeng Yi‐tao, Huang Shu‐zheng, P. K. Sukumaran, S. Miwa, G. D. Efremov, G. Petkov, G. V. Sciarratta & G. Sansone. (2006) The occurrence of different levels of G γ chain and of the A γ T variant of fetal hemoglobin in newborn babies from several countries . American Journal of Hematology 14:2, pages 133-148.
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