{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,5]],"date-time":"2025-10-05T18:11:58Z","timestamp":1759687918461,"version":"build-2065373602"},"reference-count":18,"publisher":"BMJ","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1985,8]]},"abstract":"<jats:p>A total of 102 apparently healthy and randomly selected Turks who either immigrated from Western Thrace or were still living there were studied for haemoglobin variants, high Hb A2 beta thalassaemia, G6PD deficiency, and haptoglobin types. The incidence of haemoglobins S and O Arab were 2.9 and 3.9% respectively. The incidence of high A2 beta thalassaemia was 10.8% and that of G6PD deficiency 5%. The gene frequencies of Hp1 and Hp2 were 0.326 and 0.674, respectively.<\/jats:p>","DOI":"10.1136\/jmg.22.4.288","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:09:16Z","timestamp":1226329756000},"page":"288-290","source":"Crossref","is-referenced-by-count":18,"title":["Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace."],"prefix":"10.1136","volume":"22","author":[{"given":"M","family":"Aksoy","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Kutlar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F","family":"Kutlar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G","family":"Din\u00e7ol","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S","family":"Erdem","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S","family":"Ba\u015ftesbih\u00e7i","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1985,8,1]]},"reference":[{"issue":"30","key":"ref_1","first-page":"3","article-title":"Erdem $. Survey on hacmoglobin variants, 1-thalassacmia, glucose-6-phosphatc dchydrogcnase dcficicncy and haptoglohin types in Turkish pcopic living in Manavgat","volume":"1980","author":"G, Aksoy M.Dingol","unstructured":"Aksoy M. Dingol G, Erdem $. Survey on hacmoglobin variants, 1-thalassacmia, glucose-6-phosphatc dchydrogcnase dcficicncy and haptoglohin types in Turkish pcopic living in Manavgat. Serik and Boztcpc (Antailya). Huin Hered 1980:,30:3-6.","journal-title":"Serik and Boztcpc (Antailya). Huin Hered"},{"key":"ref_2","first-page":"82","article-title":"The hemoglobinopathies. 7echniques ofidentification","author":"Huisman, T.H.J.; Jonxis, J.H.P.","year":"1977","unstructured":"Huisman THJ, Jonxis JHP. The hemoglobinopathies. 7echniques ofidentification. New York: Marcel Dekkcr, 1977:82-112."},{"issue":"193","key":"ref_3","first-page":"\"786","article-title":"Hacm-noglohin S aind E in T urkish pcoplc","volume":"1962","author":"Aksoy, M.","year":"1975","unstructured":"Aksoy M. Hacm-noglohin S aind E in T urkish pcoplc. Nature 1962:193:786-7. 4 (,avdar AO. Arcatsov A. Thalasscmia and abhiormal helmnoglohins in Turkcy. In: Aksov M, cd. Intirtiatiotial Istanlbul.sroiipo.siinttl otn abtiormnal hemoglobins and( thalas.seslcia. Ankara: TFIBITAK Ptublicationis, 1975:337-42.","journal-title":"Nature; Thalasscmia and abhiormal helmnoglohins in Turkcy. In: Aksov M, cd. Intirtiatiotial Istanlbul.sroiipo.siinttl otn abtiormnal hemoglobins and( thalas.seslcia"},{"key":"ref_4","article-title":"A suirvcy tor hcnoglohin variants and high","volume-title":"A, (3-thalassemia in 11(11)(; Iluism an THJl. cd s. Nortli Cypru.s sX'nposi.int Onl thalassemia and abnormal hemoglobins","author":"Dincol, G.; Aksoy, M.; Dingol, K.; Kutlar, A.","year":"1984","unstructured":"Dincol G, Aksoy M, Dingol K, Kutlar A. A suirvcy tor hcnoglohin variants and high A, (3-thalassemia in 11(11)( Turks. In: Aksoy M, Iluism an THJl. cd s. Nortli Cypru.s sX'nposi.int Onl thalassemia and abnormal hemoglobins, 1984 (in press)."},{"issue":"185-2","key":"ref_5","first-page":"1262","article-title":"New Istanbul Contribution to Clinical Science","volume":"12","author":"Ramot, B.; Fishers, S.; Remez, D.","year":"1978","unstructured":"New Istanbul Contribution to Clinical Science 1978;12:185-2(1). 7 Ramot B, Fishers S, Remez D, et al. Haemoglobin 0 in an Arab family. Br Med J 1960;ii: 1262-4.","journal-title":"Br Med J; Haemoglobin 0 in an Arab family"},{"issue":"1","key":"ref_6","first-page":"189","article-title":"Hlacmoglobin E in Egypt","volume":"196","author":"Hloerman, K.C.; Katmel, K.; Awinv, A.Y.","year":"1967","unstructured":"Hloerman KC, Katmel K, Awinv AY. Hlacmoglobin E in Egypt. Nature 196(1:189:69-7(1. Bairakat A. Morcngc-Rowc AJ. Gaffncv PJ. et al. Hlacrnoglohin 0 Arah in Egypt and Aden: possiblc crrors rcsulting from the usc of haenmoglohin variants as gcnctic markers in population survcys. 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Hiemioglobin 1981;5:743-6.","journal-title":"et"},{"key":"ref_9","first-page":"158","article-title":"HIacnmoglohin 0 Arah (131 21 Gilol-Lys) in Tur-kish Cypriot population","volume":"21","year":"1984","unstructured":"2Cimi $, Akar N, Arcasoy A. (,avdar AO. Dedco.lOu S. HIacnmoglohin 0 Arah (131 21 Gilol-Lys) in Tur-kish Cypriot population. J Med (Geniet 1984:21:158.","journal-title":"J Med (Geniet"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"1417","DOI":"10.1056\/NEJM197012242832601","article-title":"Hcmoglohin 0 Arab in four negro familics and its interaction with hemoglohin S and hemoglobin C","volume":"283","author":"Milncr, P.F.; Grey, Milner C.; R.","year":"1970","unstructured":"Milncr PF, Milner C Grey R, et al. Hcmoglohin 0 Arab in four negro familics and its interaction with hemoglohin S and hemoglobin C. N EngI J Med 1970;283:1417-25.","journal-title":"N EngI J Med"},{"key":"ref_11","first-page":"93","article-title":"6th meeting, Athcns, 1981: 182. 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