K Taysi, K Tinaztepe. Show Affiliations »
Abstract
Entities: Disease
Mesh： See more » Abnormalities, Multiple/geneticsBrain/abnormalitiesChromosomes, Human, 13-15Eye AbnormalitiesFace/abnormalitiesHumansInfant, NewbornKaryotypingMaleNose/abnormalitiesOrbit/abnormalitiesTrisomy
Year: 1972 PMID： 4628606 DOI： 10.1001/archpedi.1972.02110170088014
Source DB: PubMed Journal: Am J Dis Child ISSN： 0002-922X