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

Year Number of Results
1963 1
1964 1
1970 3
1971 2
1972 2
1973 1
1974 3
1975 6
1976 2
1977 3
1978 6
1980 2
1981 7
1982 13
1983 5
1984 5
1985 7
1986 4
1987 6
1988 6
1989 4
1990 3
1991 5
1992 4
1993 3
1994 5
1995 3
1996 4
1997 3
1998 5
1999 4
2000 4
2001 2
2002 1
2004 4
2006 1
2007 3
2008 4
2009 4
2010 3
2011 5
2012 1
2013 2
2014 2
2015 2
2016 4
2017 7
2018 4
2019 6
2020 3
2021 3
2022 6
2023 1
2024 0

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Similar articles for PMID: 7446562

190 results

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Page 1
Familial Gordon syndrome associated with a PIEZO2 mutation.
Alisch F, Weichert A, Kalache K, Paradiso V, Longardt AC, Dame C, Hoffmann K, Horn D. Alisch F, et al. Am J Med Genet A. 2017 Jan;173(1):254-259. doi: 10.1002/ajmg.a.37997. Epub 2016 Oct 7. Am J Med Genet A. 2017. PMID: 27714920 Review.
Genetic aspects of arthrogryposis.
Hall JG. Hall JG. Clin Orthop Relat Res. 1985 Apr;(194):44-53. Clin Orthop Relat Res. 1985. PMID: 3978933
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
McMillin MJ, Beck AE, Chong JX, Shively KM, Buckingham KJ, Gildersleeve HI, Aracena MI, Aylsworth AS, Bitoun P, Carey JC, Clericuzio CL, Crow YJ, Curry CJ, Devriendt K, Everman DB, Fryer A, Gibson K, Giovannucci Uzielli ML, Graham JM Jr, Hall JG, Hecht JT, Heidenreich RA, Hurst JA, Irani S, Krapels IP, Leroy JG, Mowat D, Plant GT, Robertson SP, Schorry EK, Scott RH, Seaver LH, Sherr E, Splitt M, Stewart H, Stumpel C, Temel SG, Weaver DD, Whiteford M, Williams MS, Tabor HK, Smith JD, Shendure J, Nickerson DA; University of Washington Center for Mendelian Genomics; Bamshad MJ. McMillin MJ, et al. Am J Hum Genet. 2014 May 1;94(5):734-44. doi: 10.1016/j.ajhg.2014.03.015. Epub 2014 Apr 10. Am J Hum Genet. 2014. PMID: 24726473 Free PMC article.
190 results