S Gilgenkrantz, M Teboul. Show Affiliations »
Abstract
Mesh: See more » ChildChromosomes, Human, Pair 22DiGeorge Syndrome/geneticsFemaleHumansTranslocation, GeneticTurner Syndrome/geneticsX Chromosome
Year: 1990 PMID: 2095774 PMCID: PMC1017287 DOI: 10.1136/jmg.27.12.791-a
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318