β-Globin gene cluster haplotypes of Hb D-Los Angeles in Mazandaran Province, Iran
Author:
Affiliation:
1. Thalassemia Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences
2. Sina Mehr Research Center
Publisher
Genetics Society of Japan
Subject
Genetics,Molecular Biology,General Medicine
Reference13 articles.
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2. Hardison, R. C., Chui, D. H. K., Riemer, C. R., Miller, W., Carver, M. F. H., Molchanova, T. P., Efremov, G. D., and Huisman, T. H. J. (1998a) Access to “A Syllabus of Human Hemoglobin Variants (1996)” via the World Wide Web. Hemoglobin 22, 113–127.
3. Hardison, R., Riemer, C., Chui, D. H. K., Huisman, T. H. J., and Miller, W. (1998b) Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulation. Genomics 47, 429–437.
4. Huisman, T. H. J., Carver, M. F. H., and Efremov, G. D. (1996) A Syllabus of Human Hemoglobin Variants. The Sickle Cell Anemia Foundation, Augusta, GA.
5. Itano, H. A. (1951) A third abnormal hemoglobin associated with hereditary hemolytic anemia. Proc. Natl. Acad. Sci. USA 37, 775–784.
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