E D'Hoore, F Gullotta. Show Affiliations »
Abstract
Entities: Chemical Disease
Mesh: See more » Abnormalities, Multiple/pathologyCalcinosis/pathologyChromosomes, Human, 6-12 and XDemyelinating Diseases/pathologyDwarfism/pathologyFemaleHumansInfantInfant, NewbornMicrocephaly/pathologyNeuroglia/pathologyTrisomy
Year: 1971 PMID: 5093130 DOI: 10.1007/bf00688444
Source DB: PubMed Journal: Acta Neuropathol ISSN: 0001-6322 Impact factor: 17.088