O P Hornstein, H D Rott, G Schwanitz, G Grosse. Show Affiliations »
Abstract
Entities: Disease
Mesh： See more » Abnormalities, Multiple/etiologyAdultAffective Symptoms/etiologyBiopsyBone and Bones/abnormalitiesCell DivisionChromosome MappingDermatoglyphicsGigantism/etiologyHaploidyHumansIntellectual Disability/etiologyKaryotypingKlinefelter Syndrome/complicationsKlinefelter Syndrome/diagnosisKlinefelter Syndrome/geneticsMalePelvic Bones/pathologySex Chromatin/analysisSex Chromosomes/analysisSpermatogenesisTestis/pathology
Year: 1974 PMID： 4812419 DOI： 10.1055/s-0028-1107741
Source DB: PubMed Journal: Dtsch Med Wochenschr ISSN： 0012-0472 Impact factor: 0.628