[1]
Ramalingam, S., Ganapathy, S., Kanchepalli, J., Jayaraj, V. and Mariyappa, M. 2025. 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. 9, 1 (May 2025). DOI:https://doi.org/10.31383/ga.vol9iss1ga04.