Unveiling a rare genetic aberration: A case study of Prader-Willi syndrome (PWS) with atypical 15q11.2-q13.3 deletion: PWS Extended Deletion of 15q11.2-q13.3 . GenApp [Internet]. 2025 May 29 [cited 2026 Oct. 10];9(1). Available from: https://genapp.ba/editions/index.php/journal/article/view/232