R L Neu, S R Assemany, L I Gardner. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChromosomesEye AbnormalitiesFemaleHumansInfantKaryotyping
Year: 1970 PMID: 4191572 DOI: 10.1016/s0140-6736(70)91072-x
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321