G Kovacs, M Freund, A Georgii. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Chromosome DeletionChromosomes, Human, 1-3Chromosomes, Human, 6-12 and XFemaleHumansKaryotypingMiddle AgedPrimary Myelofibrosis/geneticsPrimary Myelofibrosis/pathologyTrisomy
Year: 1985 PMID: 3929536 DOI: 10.1159/000206315
Source DB: PubMed Journal: Acta Haematol ISSN: 0001-5792 Impact factor: 2.195