E Ferrante, V Brinchi, P Marioni, F Galletti. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Child, PreschoolFemaleHumansKaryotypingPrader-Willi Syndrome/geneticsSex Chromatin/analysisTrisomyX Chromosome
Year: 1986 PMID: 3713664
Source DB: PubMed Journal: Minerva Pediatr ISSN: 0026-4946 Impact factor: 1.312