Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 2
152
Views
16
CrossRef citations to date
0
Altmetric
Original

GENETIC HETEROGENEITY OF β-THALASSEMIA AT ÇUKUROVA IN SOUTHERN TURKEY

, , , , , & show all
Pages 241-245 | Received 09 Jun 2000, Accepted 09 Jun 2000, Published online: 07 Jul 2009

REFERENCES

  • Yüregir G. T., Arpaci A., Aksoy K., Tuli A., Dikmen N., Özgönen T., Kilinç Y. Population at risk for hemoglobinopathies in Çukurova.Turkey; need for prenatal diagnosis. Ann. Med. Sci. 1995; 4: 61–69
  • Kohn J. Separation of hemoglobin on cellulose acetate. J. Clin. Pathol. 1969; 22: 109–110
  • Efremov G. D. Quantitation of hemoglobins by microchromatography. The Hemoglobinopathies, T. H.J. Huisman. Churchill Livingstone, EdinburghScotland 1986; 15: 72–90, Methods in Hematology
  • Singer K., Chernoff A., Singer L. Studies on abnormal hemoglobins. I. Alkali denaturation. Blood 1951; 6: 413–423
  • Poncz M., Solowiejczyk D., Harpel B., Mory Y., Schwartz E., Surrey S. Construction of human gene libraries from small amounts of peripheralblood: Analysis of β-like Globin Genes. Hemoglobin 1982; 6 (1): 27–36
  • Old J. M., Varawalla N. Y., Weatherall D. J. Rapid detection and prenatal diagnosis of β-thalassaemiastudies in Indian and Cypriot population in the UK. The Lancet 1990; 336 (8719): 834–837
  • Newton C. R., Graham A., Heptinstall L. E., Powell S. J., Summers C., Kalsheker N., Smith J. C., Markham A. F. Analysis of any point mutation in DNA. The amplification refractorymutation system (ARMS). NucleicAcids Res. 1989; 17: 2503–2516
  • Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain terminating inhibitors. Proc. Natl. Acad. Sci. USA 1977; 74: 5463–5467
  • Öner R., Altay Ç., Aksoy M., Kilinç Y., Stoming T. A., Reese A. L., Kutlar A., Kutlar F., Huisman T. H.J. β-Thalassemia in Turkey. Hemoglobin 1990; 14 (1): 1–13
  • Aulehlα-Scholz C., Basaran S., Agaoglu L., Arcasoy A., Holzgreve W., Miny P., Ridolfi F., Horst J. Molecular basis of β-thalassemia in Turkey: detection ofrare mutation by direct sequencing. Hum. Genet. 1990; 84 (2): 195–197
  • Başak A. N., Özçelik H., Özer A., Tolun A., Aksoy M., Agaoglu L., Ridolfi F., Ulukutlu L., Akar N., Gürgey A., Kýrdar B. Themolecular basis of β-thalassemia in Turkey. Hum. Genet. 1992; 89: 315–318
  • Başak A. N., Özer A., Özçelik H., Kirdar B., Gürgey A. A novel frameshift mutation: deletion of C in codons 74/75 ofthe β-globin gene causes b0-thalassemia in a Turkish Patient. Hemoglobin 1992; 16 (4): 309–312
  • Baysal E., Carver M. F.H. The β- and d-thalassemia repository. Hemoglobin 1995; 19 (3&4): 213–236
  • Ribeiro M. L.S., Baysal E., Kutlar F., Tamagnini G. P., Gonçalves P., Lopes D., Huisman T. H.J. A novel β0-thalassemia mutation(codon 15, TGG→TGA) is prevalent in a population of Central Portugal. Br. J. Haematol. 1992; 80: 567–568
  • Çürük M. A., Kutlar A., Huisman T. H.J. Hb Shelby [α2β2131(H9)Gly→Lys]-β0-thalassemia[codon 15 (TGG→TGA) identified by DNA sequencing. Hemoglobin 1992; 16 (5): 417–419

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.