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Items: 3

1.
IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration
Rachayata Dharmat, Wei Liu, Zhongqi Ge, Zixi Sun, Lizhu Yang, Yumei Li, Keqing Wang, Kandace Thomas, Ruifang Sui, Rui Chen
Invest Ophthalmol Vis Sci. 2017 May; 58(5): 2483–2490. doi: 10.1167/iovs.16-19133
PMCID:
PMC5413215
AbstractArticlePDF–1.0M
2.
A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.
M Papaioannou, D Bessant, A Payne, J Bellingham, C Rougas, A Loutradis-Anagnostou, C Gregory-Evans, A Balassopoulou, S Bhattacharya
J Med Genet. 1998 May; 35(5): 429–431. doi: 10.1136/jmg.35.5.429
PMCID:
PMC1051321
SummaryPage BrowsePDF–536K
3.
Cone and cone-rod dystrophies.
A T Moore
J Med Genet. 1992 May; 29(5): 289–290. doi: 10.1136/jmg.29.5.289
PMCID:
PMC1015945
SummaryPage BrowsePDF–372K

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