| Literature DB >> 2066420 |
Abstract
Hereditary spherocytosis is a relatively common haematological disorder and will be encountered by all haematologists. The abundance of new information, dealing principally with molecular and genetic aspects of pathophysiology, is beginning to have implications for its investigation and management. While these advances have not yet exerted a large influence at therapeutic level, the promise of such advents as prenatal diagnosis make this an exciting field to watch.Entities:
Mesh:
Year: 1991 PMID: 2066420 PMCID: PMC496820 DOI: 10.1136/jcp.44.6.441
Source DB: PubMed Journal: J Clin Pathol ISSN: 0021-9746 Impact factor: 3.411