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

Year Number of Results
2012 1
2013 1
2014 7
2015 4
2016 9
2017 7
2018 4
2019 8
2020 10
2021 17
2022 10
2023 17
2024 4

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85 results

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Page 1
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.
Kuht HJ, Maconachie GDE, Han J, Kessel L, van Genderen MM, McLean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov K, Bai D, Wei A, Li W, Jiao Y, Smirnov V, Choi JH, Tobin MD, Sheth V, Purohit R, Dawar B, Girach A, Strul S, May L, Chen FK, Heath Jeffery RC, Aamir A, Sano R, Jin J, Brooks BP, Kohl S, Arveiler B, Montoliu L, Engle EC, Proudlock FA, Nishad G, Pani P, Varma G, Gottlob I, Thomas MG. Kuht HJ, et al. Among authors: han j. Ophthalmology. 2022 Jun;129(6):708-718. doi: 10.1016/j.ophtha.2022.02.010. Epub 2022 Feb 11. Ophthalmology. 2022. PMID: 35157951 Free PMC article.
TUBB3 M323V Syndrome Presents with Infantile Nystagmus.
Jin S, Park SE, Won D, Lee ST, Han SH, Han J. Jin S, et al. Among authors: han j. Genes (Basel). 2021 Apr 15;12(4):575. doi: 10.3390/genes12040575. Genes (Basel). 2021. PMID: 33921132 Free PMC article. Review.
Ophthalmoplegia in Mitochondrial Disease.
Lee SJ, Na JH, Han J, Lee YM. Lee SJ, et al. Among authors: han j. Yonsei Med J. 2018 Dec;59(10):1190-1196. doi: 10.3349/ymj.2018.59.10.1190. Yonsei Med J. 2018. PMID: 30450853 Free PMC article.
Short Stature With Optic Atrophy and Cone Dystrophy.
Seo Y, Kim SS, Han J. Seo Y, et al. Among authors: han j. JAMA Ophthalmol. 2021 Aug 1;139(8):910-911. doi: 10.1001/jamaophthalmol.2020.5777. JAMA Ophthalmol. 2021. PMID: 34110364 No abstract available.
Clinical utility gene card for FRMD7-related infantile nystagmus.
Dawar B, Kuht HJ, Han J, Maconachie GDE, Thomas MG. Dawar B, et al. Among authors: han j. Eur J Hum Genet. 2021 Oct;29(10):1584-1588. doi: 10.1038/s41431-021-00826-9. Epub 2021 Feb 25. Eur J Hum Genet. 2021. PMID: 33633368 Free PMC article. No abstract available.
85 results