Umair, M., Ballow, M., Asiri, A., Alyafee, Y., al Tuwaijri, A., Alhamoudi, K. M., . . . Alfadhel, M. (2020). EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay. Clin Genet.
Citação norma ChicagoUmair, Muhammad, et al. "EMC10 Homozygous Variant Identified in a Family With Global Developmental Delay, Mild Intellectual Disability, and Speech Delay." Clin Genet 2020.
ציטוט MLAUmair, Muhammad, et al. "EMC10 Homozygous Variant Identified in a Family With Global Developmental Delay, Mild Intellectual Disability, and Speech Delay." Clin Genet 2020.
אזהרה: ציטוטים אלה לעיתים לא מדויקים ב 100%.