N E Simpson. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsAdolescentAdultBone and Bones/abnormalitiesCell DivisionChildChromosome AberrationsChromosome DisordersFace/abnormalitiesHumansIntellectual DisabilityKaryotypingMaleSyndrome/geneticsTestis/cytology
Year: 1973 PMID: 4735812 PMCID: PMC1762544
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025