F Egli, G Stalder. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AutopsyChromosome AberrationsChromosomes, Human, 13-15Chromosomes, Human, 16-18Chromosomes, Human, 21-22 and YChromosomes, Human, 4-5Cri-du-Chat SyndromeFemaleGenetics, PopulationHumansInfant, NewbornKidney/abnormalitiesKlinefelter SyndromeMaleTrisomyTurner SyndromeUrinary Tract/abnormalities
Year: 1973 PMID: 4578678 DOI: 10.1007/bf00279026
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348