RAMALINGAM, S.; GANAPATHY, S.; KANCHEPALLI, J.; JAYARAJ, V.; MARIYAPPA, M. 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 . Genetics & Applications, [S. l.], v. 9, n. 1, 2025. DOI: 10.31383/ga.vol9iss1ga04. Disponível em: https://genapp.ba/editions/index.php/journal/article/view/232. Acesso em: 17 oct. 2025.