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Results by year

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

Year Number of Results
1902 1
1913 1
1918 1
1922 1
1945 1
1950 1
1954 1
1957 1
1959 1
1963 1
1968 1
1976 1
1978 1
1979 1
1980 2
1982 2
1984 1
1985 1
1986 3
1987 1
1988 1
1990 2
1991 1
1993 1
1994 1
1995 1
1996 1
1998 2
1999 2
2000 7
2001 4
2002 8
2003 7
2004 9
2005 7
2006 8
2007 10
2008 10
2009 12
2010 9
2011 15
2012 3
2013 17
2014 21
2015 21
2016 19
2017 32
2018 19
2019 20
2020 17
2021 18
2022 21
2023 13
2024 2

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Similar articles for PMID: 25173900

316 results

Results by year

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Page 1
CCDD Phenotype Associated with a Small Chromosome 2 Deletion.
Abu-Amero KK, Bosley TM, Kondkar AA, Oystreck DT, Khan AO. Abu-Amero KK, et al. Semin Ophthalmol. 2015;30(5-6):435-42. doi: 10.3109/08820538.2013.874474. Epub 2014 Jan 29. Semin Ophthalmol. 2015. PMID: 24475916
The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis.
Dieterich K, Quijano-Roy S, Monnier N, Zhou J, Fauré J, Smirnow DA, Carlier R, Laroche C, Marcorelles P, Mercier S, Mégarbané A, Odent S, Romero N, Sternberg D, Marty I, Estournet B, Jouk PS, Melki J, Lunardi J. Dieterich K, et al. Hum Mol Genet. 2013 Apr 15;22(8):1483-92. doi: 10.1093/hmg/dds514. Epub 2012 Dec 11. Hum Mol Genet. 2013. PMID: 23236030
Mutations in ECEL1 cause distal arthrogryposis type 5D.
McMillin MJ, Below JE, Shively KM, Beck AE, Gildersleeve HI, Pinner J, Gogola GR, Hecht JT, Grange DK, Harris DJ, Earl DL, Jagadeesh S, Mehta SG, Robertson SP, Swanson JM, Faustman EM, Mefford HC, Shendure J, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics. McMillin MJ, et al. Am J Hum Genet. 2013 Jan 10;92(1):150-6. doi: 10.1016/j.ajhg.2012.11.014. Epub 2012 Dec 20. Am J Hum Genet. 2013. PMID: 23261301 Free PMC article.
316 results