References
- Huisman T. H.J., Carver M. F.H., Efremov G. D. A Syllabus of Human Hemoglobin Variants (second edition). The Sickle Cell Anemia Foundation, Augusta GAUSA 1998
- Moo-Penn W. F., Jue D. L., Johnson M. H., Wilson S. H., Therrell B., Schmidt R. M. Hemoglobin Tarrant: αl26(H9) Asp→Asn. A new hemoglobin variant in the α1β1 contact region showing high oxygen affinity and reduced cooperativity. Biochim. Biophys. Acta 1977; 490: 443–451
- Ibarra B., Vaca G., Cantu J. M., Wilson J. B., Lam H., Stallings M., Gravely M. E., Huisman T. H. J. Heterozygosity and homozygosity for the high oxygen affinity Hemoglobin Tarrant or α126(H9)Asp→-Asn in two Mexican families. Hemoglobin 1982; 5: 337–348
- Schroeder W. A., Shelton J. B., Shelton J. R., Powars D., Friedman S., Baker J., Finkle-Stein J. Z., Miller B., Johnson C. S., Sharpsteen J. R., Sieger L., Kawaoka E. Identification of eleven human hemoglobin variants by high-performance liquid chromatography: Additional data on functional properties and clinical expression. Biochem. Genet. 1982; 20: 133–152
- Huisman T. H.J, Jonxis J. H.P. The Hemoglobinopathies Techniques of Ientification. Clinical and Biochemical Analysis. Marcel Dekker Inc., New York NYUSA 1977; Vol. 6
- Miller S. A., Dykes D. D., Polesky H. F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988; 16: 1215–1216
- Dodé C., Rochette J., Krishnamoorthy R. Locus assignment of human α globin mutations by selective amplification and direct sequencing. Br. J. Haematol. 1990; 76: 275–281
- Singer K., Chernoff A. I., Singer L. Studies on Abnormal Hemoglobins. I. Their demonstration in sickle cell anemia and other hematological disorders by means of alkali denaturation. Blood 1951; 6: 413–428