Open Access 01.12.2023 | Correction
Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
Erschienen in: Italian Journal of Pediatrics | Ausgabe 1/2023
Open Access 01.12.2023 | Correction
Erschienen in: Italian Journal of Pediatrics | Ausgabe 1/2023