توثيق جمعية علم النفس الأمريكية APA (الطبعة السابعة)

Yusuf, I., Gliem, M., Birtel, J., Muller, P., Mangold, E., Bolz, H., & Issa, P. (2018). The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1. Association for Research in Vision and Ophthalmology.

توثيق أسلوب شيكاغو (الطبعة السابعة عشر)

Yusuf, IH, M. Gliem, J. Birtel, PL Muller, E. Mangold, H. Bolz, و PC Issa. The Retinal Phenotype Associated with the Frequent, Synonymous C.783G > A Mutation in CDHR1. Association for Research in Vision and Ophthalmology, 2018.

توثيق جمعية اللغة المعاصرة MLA (الإصدار التاسع)

Yusuf, IH, et al. The Retinal Phenotype Associated with the Frequent, Synonymous C.783G > A Mutation in CDHR1. Association for Research in Vision and Ophthalmology, 2018.