APA استشهاد

Chao, H., Davids, M., Burke, E., Pappas, J. G., Rosenfeld, J. A., McCarty, A. J., . . . Malicdan, M. C. V. (2017). A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. Am J Hum Genet.

استشهاد بنمط شيكاغو

Chao, Hsiao-Tuan, et al. "A Syndromic Neurodevelopmental Disorder Caused By De Novo Variants in EBF3." Am J Hum Genet 2017.

MLA استشهاد

Chao, Hsiao-Tuan, et al. "A Syndromic Neurodevelopmental Disorder Caused By De Novo Variants in EBF3." Am J Hum Genet 2017.

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