J Q Miller, R F Selden. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Brain/pathologyChromosomes, Human, 13-15Congenital Abnormalities/pathologyEncephalocele/complicationsHumansInfant, NewbornKaryotypingLimbic System/abnormalitiesTrisomy
Year: 1967 PMID: 6069295 DOI: 10.1212/wnl.17.11.1087
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910