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Translational Vision Science & Technology|June 15, 2021
Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 GeneHiroyuki Kondo, Itsuka Matsushita, Tatsuo Nagata, et al.
Human Genome Variation|November 1, 2019
Retinal structure in Leber's congenital amaurosis caused by RPGRIP1 mutationsDaisuke Miyamichi, Sachiko Nishina, Katsuhiro Hosono, et al.
Japanese Journal of Ophthalmology|April 19, 2018
Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutationsKentaro Kurata, Katsuhiro Hosono, Akiko Hikoya, et al.
Retina (Philadelphia, Pa.)|August 12, 2017
ATYPICAL FORM OF RETINOPATHY OF PREMATURITY WITH SEVERE FIBROVASCULAR PROLIFERATION IN THE OPTIC DISK REGIONTadashi Yokoi, Satoshi Katagiri, Miina Hiraoka, et al.
Ophthalmology|March 4, 2006
Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophyMakoto Nakamura, Jian Lin, Shinji Ueno, et al.
Journal of Human Genetics|September 17, 2010
Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1Hiroshi Nakanishi, Masafumi Ohtsubo, Satoshi Iwasaki, et al.
Human Genome Variation|June 9, 2016
Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacyChunxia Wang, Katsuhiro Hosono, Shu Kachi, et al.
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