“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, vol. 9, no. 1, May 2025, doi: 10.31383/ga.vol9iss1ga04.