{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T00:16:58Z","timestamp":1760833018189,"version":"build-2065373602"},"reference-count":15,"publisher":"BMJ","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1979,12]]},"abstract":"<jats:p>A study is presented on eleven patients with homozygous sickle cell anaemia. They are non-Sheeah Arabs from the United Arab Emirates on the south-eastern coast of the Arabian Peninsula. The proportions of fetal haemoglobin in these patients are variable, and there is a marked variation in the severity of their disease condition; these facts are not related. African sickle cell gene admixture is a likely affecting factor.<\/jats:p>","DOI":"10.1136\/jmg.16.6.428","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T14:50:51Z","timestamp":1226328651000},"page":"428-430","source":"Crossref","is-referenced-by-count":9,"title":["Heterogeneity of sickle cell anaemia in Arabs: review of cases with various amounts of fetal haemoglobin."],"prefix":"10.1136","volume":"16","author":[{"given":"K","family":"Kamel","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1979,12,1]]},"reference":[{"key":"ref_1","first-page":"38","article-title":"The United Arab Emirates. A Modern History","author":"Abdullah, M.M.","year":"1978","unstructured":"Abdullah, M. M. (1978). The United Arab Emirates. A Modern History, p. 38. Harper and Row, USA."},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1182\/blood.V28.4.553.553","article-title":"A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency, and glutathione reductase deficiency","volume":"28","author":"Beutler, E.","year":"1966","unstructured":"Beutler, E. (1966). A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency, and glutathione reductase deficiency. Blood, 28, 553-562.","journal-title":"Blood"},{"key":"ref_3","first-page":"238","article-title":"Practical Haematology","author":"Dacie, J.V.; Lewis, S.M.","year":"1975","unstructured":"Dacie, J. V., and Lewis, S. M. (1975). Practical Haematology, 5th ed., pp. 238-243. 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Economics and Political Evolution in the Arabian Gulf States, p. 45. Carlton Press, New York."},{"key":"ref_13","article-title":"Studies on abnormal hemoglobins","author":"Singer, K.; Chernoff, A.; Singer, L.","year":"1951","unstructured":"Singer, K., Chernoff, A., and Singer, L. (1951). Studies on abnormal hemoglobins."},{"key":"ref_14","first-page":"\"413","article-title":"Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation","volume":"6","author":"Weatherall, D.J.; Clegg, J.B.","year":"1972","unstructured":"Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation. Blood, 6, 413-428. Weatherall, D. J., and Clegg, J. B. (1972). The Thalassaemia Syndromes, 2nd ed., p. 311. Blackwell Scientific Publications, Oxford.","edition":"2nd ed","journal-title":"Blood; The Thalassaemia Syndromes"},{"key":"ref_15","series-title":"Series","first-page":"9","article-title":"Nutritional anemias. 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