L G Macdougall, J A Brown, M M Cohen, J M Judisch. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Chromosome AberrationsChromosomes, Human, 6-12 and XCytogeneticsFemaleHumansInfantKaryotypingMyeloproliferative Disorders/genetics
Year: 1974 PMID: 4810736 DOI: 10.1016/s0022-3476(74)80616-5
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406