O Robain, G Lyon. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Brain/abnormalitiesCerebral Cortex/abnormalitiesCerebral Cortex/pathologyCorpus Callosum/pathologyFemaleFrontal Lobe/pathologyHumansInfantInfant, NewbornMaleMicrocephaly/etiologyMicrocephaly/geneticsMicrocephaly/pathologyParietal Lobe/pathology
Year: 1972 PMID: 5018226 DOI: 10.1007/BF00691127
Source DB: PubMed Journal: Acta Neuropathol ISSN: 0001-6322 Impact factor: 17.088