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

Year Number of Results
1981 1
1982 1
1986 1
1989 1
1990 1
1991 1
1992 4
1993 4
1994 1
1995 2
1997 1
1998 1
1999 3
2000 2
2001 1
2002 1
2016 2
2021 2
2023 1

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31 results

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Page 1
Genotype-phenotype correlations in X-linked myotubular myopathy.
McEntagart M, Parsons G, Buj-Bello A, Biancalana V, Fenton I, Little M, Krawczak M, Thomas N, Herman G, Clarke A, Wallgren-Pettersson C. McEntagart M, et al. Among authors: fenton i. Neuromuscul Disord. 2002 Dec;12(10):939-46. doi: 10.1016/s0960-8966(02)00153-0. Neuromuscul Disord. 2002. PMID: 12467749
Genetic heterogeneity in X-linked amelogenesis imperfecta.
Aldred MJ, Crawford PJ, Roberts E, Gillespie CM, Thomas NS, Fenton I, Sandkuijl LA, Harper PS. Aldred MJ, et al. Among authors: fenton i. Genomics. 1992 Nov;14(3):567-73. doi: 10.1016/s0888-7543(05)80153-3. Genomics. 1992. PMID: 1358807
A full genome scan for late onset Alzheimer's disease.
Kehoe P, Wavrant-De Vrieze F, Crook R, Wu WS, Holmans P, Fenton I, Spurlock G, Norton N, Williams H, Williams N, Lovestone S, Perez-Tur J, Hutton M, Chartier-Harlin MC, Shears S, Roehl K, Booth J, Van Voorst W, Ramic D, Williams J, Goate A, Hardy J, Owen MJ. Kehoe P, et al. Among authors: fenton i. Hum Mol Genet. 1999 Feb;8(2):237-45. doi: 10.1093/hmg/8.2.237. Hum Mol Genet. 1999. PMID: 9931331
31 results