APA (7th ed.) Citation

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. University of Sarajevo, Institute for Genetic Engineering and Biotechnology.

Chicago Style (17th ed.) Citation

Ramalingam, Senthilraja, Srividya Ganapathy, Jayaswathi Kanchepalli, Vani Jayaraj, and Mani Mariyappa. Unveiling a Rare Genetic Aberration: A Case Study of Prader-Willi Syndrome (PWS) with Atypical 15q11.2-q13.3 Deletion. University of Sarajevo, Institute for Genetic Engineering and Biotechnology.

MLA (9th ed.) Citation

Ramalingam, Senthilraja, et al. Unveiling a Rare Genetic Aberration: A Case Study of Prader-Willi Syndrome (PWS) with Atypical 15q11.2-q13.3 Deletion. University of Sarajevo, Institute for Genetic Engineering and Biotechnology.