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
- Casals T., Baiget M., Hernandez J. L. Asociación Hb D Punjab/β0-talasemia: primer caso en España. Sangre 1986; 31: 483–488
- Sáenz-Renauld G. F., Rodriguez-Romero W., Chaves-Villalobos M. Variantes estructurales de la hemoglobina en Iberoamérica. Rev. Biol. Trop. 1993; 41: 393–402
- Ruiz-Reyes G. Hemoglobinas anormales y talasemias en la Républica Mexicana. Rev. Invest. Clin. 1998; 50: 163–170
- Bunn H. F., Forget B. G. Hemoglobin: Molecular, Genetic and Clinical Aspects. W.B. Saunders Company, Philadelphia PAUSA 1986
- Huisman T. H.J, Jonxis J. The Hemoglobinopathies Techniques of Identification. 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
- Varawalla N. Y., Old J. M., Sarkar R., Venkatesan R., Weatherall D. J. The spectrum of β-thalassaemia mutations on the Indian Subcontinent: the basis for prenatal diagnosis. Br. J. Haematol. 1991; 78: 242–247
- Varawalla N. Y., Fitches A. C., Old J. M. Analysis of β-globin gene haplotype in Asian Indian: origin and spread of β-thalassaemia on the Indian Subcontinent. Hum. Genet. 1992; 90: 443–449
- Weatherall D. J., Clegg J. B., Higgs D. R., Wood W. G. The hemoglobinopathies. The Metabolic and Molecular Bases of Inherited Disease, 7th edition, C. R. Scriver, A. L. Beadut, W. S. Sly, D. Valle. McGraw Hill, Inc., New York NYUSA 1995; 3417–3484
- Adachi K., Kim J., Ballas S., Surrey S., Asakura T. Facilitation of Hb S polymerization by the substitution of Glu for Gin at βl21. J. Biol. Chem. 1988; 263: 5607–5610
- Adekile A. D., Kazanetz E. G., Leonova J. Y., Marouf R., Khmis A., Huisman T. H.J. Co-inheritance of Hb D-Punjab (codon 121; GAA→CAA) and β0-thalassemia (IVS-II-1; G→A). J. Pediatr. Hematol. Oncol. 1996; 18: 151–153
- Peñaloza R., Garcia-Carranca A., Ceras T., Alvarez C., Berumen J., Zavala C., Salamanca F. Frequency of hapotypes in the β globin gene cluster in a selected sample of the Mexican population. Am. J. Hum. Biol. 1995; 7: 45–49
- Villalobos-Arambula A. R., Bustos R., Casas-Castañeda M., Gutierrez E., Perea F. J., Thein S. L., Ibarra B. β-Tthalassemia and βA globin gene haplotypes in Mexican Mestizos. Hum. Genet. 1997; 99: 498–500
- Villalobos-Arambula A. R., Rivas F., Sandoval L., Perea F J., Casas-Castaßneda M., Cantú J. M., Ibarra B. βA Globin gene haplotypes in Mexican HuicholsGenetic relatedness to other populations. Am. J. Hum. Biol. 1999, in press
- Flint J., Harding R. M., Boyce A. J., Clegg J. B. The population genetics of the haemoglobinopathies. The Haemoglobinopathies. Bailliere's Clinical Hematology, International Practice and Research, D. R. Higgs, D. J. Weatherall. Baillière Tindall, LondonEngland 1993; 215–262
- Fioretti G., De Angioletti M., Pagano L., Lacerra G., Viola A., Bonis C., Scarallo A., Carestia C. DNA polymorphism associated with Hb D-Los Angeles (β121(GH4) Glu→Gln) in Southern Italy. Hemoglobin 1993; 17: 9–17