| Literature DB >> 6162733 |
M Horányi, J Szelényi, G Rona, A Lang, H Lehmann, S R Hollán.
Abstract
A 29-year-old Hungarian woman was found to be double heterozygote for Hb O Arab and beta-thalassaemia. Haemolytic anaemia became manifest during her second pregnancy. In the course of genetic studies G-6-PD deficiency was also detected in the family. The patient originates from a North-Eastern part of Hungary which had been hydrogeologically isolated during past centuries.Entities:
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Year: 1980 PMID： 6162733
Source DB: PubMed Journal: Folia Haematol Int Mag Klin Morphol Blutforsch ISSN： 0323-4347