APA (7th ed.) Citation

Bücking, J., An, Y., Bi, W., Hinderhofer, K., Theiß, S., Slavotinek, A., & Schaaf, C. P. (2025). A case of Prader-Willi syndrome with a deletion including MAGEL2 , NDN , and MKRN3 , but excluding SNRPN and SNORD116. American journal of medical genetics, 197(8), . https://doi.org/10.1002/ajmg.a.64070

Chicago Style (17th ed.) Citation

Bücking, Jannis, Yu An, Weimin Bi, Katrin Hinderhofer, Susanne Theiß, Anne Slavotinek, and Christian P. Schaaf. "A Case of Prader-Willi Syndrome with a Deletion Including MAGEL2 , NDN , and MKRN3 , but Excluding SNRPN and SNORD116." American Journal of Medical Genetics 197, no. 8 (2025). https://doi.org/10.1002/ajmg.a.64070.

MLA (9th ed.) Citation

Bücking, Jannis, et al. "A Case of Prader-Willi Syndrome with a Deletion Including MAGEL2 , NDN , and MKRN3 , but Excluding SNRPN and SNORD116." American Journal of Medical Genetics, vol. 197, no. 8, 2025, https://doi.org/10.1002/ajmg.a.64070.

Warning: These citations may not always be 100% accurate.