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pro vyhledávání: '"Luiza Vitan"'
Autor:
Delia-Maria Nicoară, Alexandra-Cristina Scutca, Niculina Mang, Iulius Juganaru, Andrei-Ioan Munteanu, Luiza Vitan, Otilia Mărginean
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Prader-Willi syndrome (PWS, OMIM176270) is a rare genetic disorder with recognizable dysmorphic features and multisystemic consequences such as endocrine, neurocognitive and metabolic ones. Although most patients with Prader-Willi syndrome exhibit hy
Externí odkaz:
https://doaj.org/article/e22eeddb163645d5a24503a6ec06d806
