Abstract
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 β 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 β thalassaemia was 10.8% and that of G6PD deficiency 5%. The gene frequencies of Hp1 and Hp2 were 0.326 and 0.674, respectively.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 288-290 |
| Number of pages | 3 |
| Journal | Journal of Medical Genetics |
| Volume | 22 |
| Issue number | 4 |
| State | Published - Dec 11 1985 |
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ASJC Scopus subject areas
- Genetics
- Genetics(clinical)
Cite this
Survey on haemoglobin variants, β-thalassemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from Western Thrace. / Aksoy, M.; Kutlar, Abdullah; Kutlar, F.; Dinçol, G.; Erdem, S.; Baştesbihçi, S.
In: Journal of Medical Genetics, Vol. 22, No. 4, 11.12.1985, p. 288-290.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Survey on haemoglobin variants, β-thalassemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from Western Thrace
AU - Aksoy, M.
AU - Kutlar, Abdullah
AU - Kutlar, F.
AU - Dinçol, G.
AU - Erdem, S.
AU - Baştesbihçi, S.
PY - 1985/12/11
Y1 - 1985/12/11
N2 - 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 β 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 β thalassaemia was 10.8% and that of G6PD deficiency 5%. The gene frequencies of Hp1 and Hp2 were 0.326 and 0.674, respectively.
AB - 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 β 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 β thalassaemia was 10.8% and that of G6PD deficiency 5%. The gene frequencies of Hp1 and Hp2 were 0.326 and 0.674, respectively.
UR - http://www.scopus.com/inward/record.url?scp=0021924902&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0021924902&partnerID=8YFLogxK
M3 - Article
C2 - 4045955
AN - SCOPUS:0021924902
VL - 22
SP - 288
EP - 290
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
SN - 0022-2593
IS - 4
ER -