R B Surana, P E Conen. Show Affiliations »
Abstract
Mesh: See more » Chromosome AberrationsChromosomes, Human, 13-15Chromosomes, Human, 16-18Chromosomes, Human, 6-12 and XCrossing Over, GeneticDermatoglyphicsFibroblasts/cytologyHumansInfantKaryotypingLymphocytes/cytologyMalePedigreePhenotype
Year: 1972 PMID: 5025473 PMCID: PMC1469191 DOI: 10.1136/jmg.9.1.105
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318