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Also preliminary data indicate that among the Omani population with sickle cell disease, homozygosity of the alpha+ gene markedly modifies the clinical picture.<\/jats:p>","DOI":"10.1136\/jmg.30.5.396","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:23:16Z","timestamp":1226330596000},"page":"396-400","source":"Crossref","is-referenced-by-count":37,"title":["Frequency and clinical significance of erythrocyte genetic abnormalities in Omanis."],"prefix":"10.1136","volume":"30","author":[{"given":"J M","family":"White","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B S","family":"Christie","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D","family":"Nam","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Daar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D R","family":"Higgs","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[1993,5,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"245","DOI":"10.1136\/jmg.23.3.245","article-title":"Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and a and P thalassaemia","volume":"23","author":"White, J.M.; Byrne, M.; Richards, R.; Buchanan, T.; Katsoulis, E.; Weerasingh, K.","year":"1986","unstructured":"White JM, Byrne M, Richards R, Buchanan T, Katsoulis E, Weerasingh K. 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