F Gullotta, H Rehder, A Gropp. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Brain/pathologyChromosome Aberrations/pathologyChromosome DisordersChromosomes, Human, 13-15Chromosomes, Human, 16-18Down Syndrome/pathologyFemaleHumansInfant, NewbornIntellectual Disability/pathologyMaleTrisomy
Year: 1981 PMID: 6456980 DOI: 10.1007/bf00281680
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132