S Moric-Petrovic, Z Laca, A Krstic, M Zivkov. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Chromosome DeletionChromosomes, Human, 13-15/ultrastructureChromosomes, Human, 19-20/ultrastructureFemaleGenetic VariationHumansInfantPhenotypePrader-Willi Syndrome/genetics
Year: 1981 PMID: 7334512 PMCID: PMC1048802 DOI: 10.1136/jmg.18.6.481
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318