Group by: Item Type | No Grouping Jump to: Article Number of items: 1. ArticleGirisha, K.M. and Vahab, S.A. and Dalal, Ashwin and Gopinath, P.M. and Satyamoorthy, K. (2010) Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis. Annals of Hematology, 89 (6). pp. 625-626. ISSN 0939-5555
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