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 شيكاغوAlhamoudi, 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 استشهادAlhamoudi, 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%.