[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Number of items: 1.

Girisha, 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

This list was generated on Sat Nov 16 19:13:32 2024 IST.