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Table representation of search results timeline featuring number of search results per year.

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1975 1
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PubMed (cited) for id: 120970

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Page 1
IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration.
Dharmat R, Liu W, Ge Z, Sun Z, Yang L, Li Y, Wang K, Thomas K, Sui R, Chen R. Dharmat R, et al. Invest Ophthalmol Vis Sci. 2017 May 1;58(5):2483-2490. doi: 10.1167/iovs.16-19133. Invest Ophthalmol Vis Sci. 2017. PMID: 28460050 Free PMC article.
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.
Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, Bellingham J, Ng D, Herbrick JA, Duncan A, Scherer SW, Tsui LC, Loutradis-Anagnostou A, Jacobson SG, Cepko CL, Bhattacharya SS, McInnes RR. Freund CL, et al. Cell. 1997 Nov 14;91(4):543-53. doi: 10.1016/s0092-8674(00)80440-7. Cell. 1997. PMID: 9390563 Free article.
Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype.
Evans K, Duvall-Young J, Fitzke FW, Arden GB, Bhattacharya SS, Bird AC. Evans K, et al. Arch Ophthalmol. 1995 Feb;113(2):195-201. doi: 10.1001/archopht.1995.01100020079033. Arch Ophthalmol. 1995. PMID: 7864751
Cone and cone-rod dystrophies.
Moore AT. Moore AT. J Med Genet. 1992 May;29(5):289-90. doi: 10.1136/jmg.29.5.289. J Med Genet. 1992. PMID: 1583653 Free PMC article. No abstract available.
11 results