H G Terheggen, R A Pfeiffer, H Haug, W Schünke. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/diagnosisBone and Bones/abnormalitiesChild, PreschoolCytogeneticsDiagnosis, DifferentialEye AbnormalitiesHumansHypogonadismInfantInfant, NewbornIntellectual DisabilityKlinefelter SyndromeMaleNervous System MalformationsSex Chromosome Aberrations/diagnosisSyndrome
Year: 1973 PMID: 4203681
Source DB: PubMed Journal: Z Kinderheilkd ISSN: 0044-2917