L S Penrose, D Loesch. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Chromosome AberrationsChromosome DisordersChromosomes, Human, 13-15Chromosomes, Human, 16-18Chromosomes, Human, 21-22 and YCri-du-Chat Syndrome/geneticsDermatoglyphicsFemaleFoot/anatomy & histologyHand/anatomy & histologyHumansKlinefelter Syndrome/geneticsMaleSex Chromosome AberrationsTrisomyTurner Syndrome/genetics
Year: 1970 PMID: 5512213 DOI: 10.1111/j.1365-2788.1970.tb01107.x
Source DB: PubMed Journal: J Ment Defic Res ISSN: 0022-264X