Unveiling a rare genetic aberration: A case study of Prader-Willi syndrome (PWS) with atypical 15q11.2-q13.3 deletion - Senthilraja Ramalingam; Srividya Ganapathy; Jayaswathi Kanchepalli; Vani Jayaraj; Mani Mariyappa (Genetics & Applications, 2025)