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Results by year

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

Year Number of Results
1971 1
1979 3
1981 1
1988 1
1990 1
1991 3
1992 1
1993 2
1994 1
1995 2
1996 8
1997 2
1998 5
1999 3
2000 1
2002 1
2003 3
2005 2
2006 1
2009 3
2010 2
2011 3
2012 4
2014 2
2015 1
2016 2
2017 1
2018 3
2019 2
2020 1
2022 1
2024 0

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PubMed (Bookshelf cited) for id: 98376

64 results

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Page 1
Acanthosis nigricans, hypochondroplasia, and FGFR3 mutations: Findings with five new patients, and a review of the literature.
Muguet Guenot L, Aubert H, Isidor B, Toutain A, Mazereeuw-Hautier J, Collet C, Bourrat E, Denis Musquer M, Barbarot S; Groupe de Recherche de la Société Française de Dermatologie Pédiatrique. Muguet Guenot L, et al. Pediatr Dermatol. 2019 Mar;36(2):242-246. doi: 10.1111/pde.13748. Epub 2019 Feb 14. Pediatr Dermatol. 2019. PMID: 30762251 Review.
A novel mutation p.Ser348Cys in FGFR3 causes achondroplasia.
Hasegawa K, Fukuhara R, Moriwake T, Tanaka H, Higuchi Y, Yamashita M, Tsukahara H. Hasegawa K, et al. Am J Med Genet A. 2016 May;170A(5):1370-2. doi: 10.1002/ajmg.a.37557. Epub 2016 Jan 11. Am J Med Genet A. 2016. PMID: 26754866 No abstract available.
Timing, rates and spectra of human germline mutation.
Rahbari R, Wuster A, Lindsay SJ, Hardwick RJ, Alexandrov LB, Turki SA, Dominiczak A, Morris A, Porteous D, Smith B, Stratton MR; UK10K Consortium; Hurles ME. Rahbari R, et al. Nat Genet. 2016 Feb;48(2):126-133. doi: 10.1038/ng.3469. Epub 2015 Dec 14. Nat Genet. 2016. PMID: 26656846 Free PMC article.
64 results