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

Year Number of Results
1936 1
1939 1
1946 1
1947 1
1948 4
1949 2
1950 4
1951 9
1952 4
1953 5
1954 2
1955 3
1957 1
1958 5
1961 3
1964 1
1966 1
1967 2
1968 1
1969 1
1970 2
1972 2
1974 3
1977 1
1978 1
1979 1
1981 1
1982 4
1983 2
1984 1
1985 1
1986 1
1987 1
1988 1
1989 4
1990 4
1991 7
1992 6
1993 7
1994 8
1995 14
1996 15
1997 10
1998 16
1999 12
2000 11
2001 16
2002 16
2003 19
2004 16
2005 26
2006 21
2007 28
2008 46
2009 41
2010 41
2011 41
2012 47
2013 40
2014 46
2015 43
2016 34
2017 54
2018 52
2019 38
2020 62
2021 56
2022 52
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Search Results

927 results
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Page 1
Usher Syndrome: Genetics of a Human Ciliopathy.
Fuster-García C, García-Bohórquez B, Rodríguez-Muñoz A, Aller E, Jaijo T, Millán JM, García-García G. Fuster-García C, et al. Int J Mol Sci. 2021 Jun 23;22(13):6723. doi: 10.3390/ijms22136723. Int J Mol Sci. 2021. PMID: 34201633 Free PMC article. Review.
Ciliopathy: Usher Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:167-170. doi: 10.1007/978-3-319-95046-4_32. Adv Exp Med Biol. 2018. PMID: 30578505 Review.
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients.
Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda KH. Koyanagi Y, et al. J Med Genet. 2019 Oct;56(10):662-670. doi: 10.1136/jmedgenet-2018-105691. Epub 2019 Jun 17. J Med Genet. 2019. PMID: 31213501
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C. Bonnet C, et al. Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27. Eur J Hum Genet. 2016. PMID: 27460420 Free PMC article.
Usher syndrome.
Hossain MM, Islam MF. Hossain MM, et al. Mymensingh Med J. 2012 Jan;21(1):155-7. Mymensingh Med J. 2012. PMID: 22314473
927 results