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.
शिकागो शैली (17वां संस्करण) प्रशस्ति पत्रYusuf, IH, M. Gliem, J. Birtel, PL Muller, E. Mangold, H. Bolz, और PC Issa. The Retinal Phenotype Associated with the Frequent, Synonymous C.783G > A Mutation in CDHR1. Association for Research in Vision and Ophthalmology, 2018.
एमएलए (9वां संस्करण) प्रशस्ति पत्रYusuf, 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.
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