A Ferrandez, W Schmid. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Abnormalities, MultipleChromosome AberrationsChromosome DisordersDigestive System AbnormalitiesFacial ExpressionHumansHyaline Membrane Disease/geneticsInfant, NewbornKaryotypingKidney/abnormalitiesLung/abnormalitiesMaleMosaicism
Year: 1971 PMID: 5139247
Source DB: PubMed Journal: Helv Paediatr Acta ISSN: 0018-022X