Chowdhury, W., Patak, P., Chowdhury, F. J., Ijaz, H. M., Zafar, T., Chatla, N., & Khiami, A. (2018). A Rare Case of 15q11.2 Microdeletion Syndrome with Atypical Features: Diagnostic Dilemma. Cureus.

Chowdhury, Waliul, Pooja Patak, Farjahan J. Chowdhury, Hasnan M. Ijaz, Tehmina Zafar, Nick Chatla, και Ahmad Khiami. "A Rare Case of 15q11.2 Microdeletion Syndrome With Atypical Features: Diagnostic Dilemma." Cureus 2018.

Chowdhury, Waliul, et al. "A Rare Case of 15q11.2 Microdeletion Syndrome With Atypical Features: Diagnostic Dilemma." Cureus 2018.