APA استشهاد

Alhamoudi, K. M., Bhat, J., Nashabat, M., Alharbi, M., Alyafee, Y., Asiri, A., . . . Alfadhel, M. (2020). A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. Front Pediatr.

استشهاد بنمط شيكاغو

Alhamoudi, Kheloud M., Javaid Bhat, Marwan Nashabat, Masheal Alharbi, Yusra Alyafee, Abdulaziz Asiri, Muhammad Umair, و Majid Alfadhel. "A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia." Front Pediatr 2020.

MLA استشهاد

Alhamoudi, Kheloud M., et al. "A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia." Front Pediatr 2020.

تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.