Now showing items 1-1 of 1

  • Saeves, Ronnaug; Espelid, Ivar; Storhaug, Kari; Sandvik, Leiv; Nordgarden, Hilde (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2012)
    Background Prader-Willi syndrome (PWS) is a rare complex multsystemic genetic disorder characterized by severe neonatal hypotonia, endocrine disturbances, hyperphagia and obesity, mild mental retardation, ...