R B Surana, P Forbath, P E Conen. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, MultipleCytogeneticsDermatoglyphicsHumansInfantIntellectual DisabilityKaryotypingMaleScrotum/abnormalitiesSex Chromosome AberrationsTestis/abnormalities
Year: 1971 PMID: 5314803
Source DB: PubMed Journal: Ann Genet ISSN: 0003-3995