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

Year Number of Results
1979 1
1996 1
1998 1
2002 1
2004 1
2008 3
2009 13
2010 12
2011 15
2012 16
2013 19
2014 17
2015 18
2016 17
2017 19
2018 4
2019 2
2020 1
2022 0
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Search Results

140 results
Results by year
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Page 1
Pelizaeus-Merzbacher disease as a chromosomal disorder.
Yamamoto T, Shimojima K. Yamamoto T, et al. Among authors: shimojima k. Congenit Anom (Kyoto). 2013 Mar;53(1):3-8. doi: 10.1111/cga.12005. Congenit Anom (Kyoto). 2013. PMID: 23480352 Review.
Clinical impacts of genomic copy number gains at Xq28.
Yamamoto T, Shimojima K, Shimada S, Yokochi K, Yoshitomi S, Yanagihara K, Imai K, Okamoto N. Yamamoto T, et al. Among authors: shimojima k. Hum Genome Var. 2014 Jul 24;1:14001. doi: 10.1038/hgv.2014.1. eCollection 2014. Hum Genome Var. 2014. PMID: 27081496 Free PMC article. Review.
Neurological manifestations of 2q31 microdeletion syndrome.
Okamoto N, Kimura S, Shimojima K, Yamamoto T. Okamoto N, et al. Among authors: shimojima k. Congenit Anom (Kyoto). 2017 Nov;57(6):197-200. doi: 10.1111/cga.12212. Epub 2017 Mar 24. Congenit Anom (Kyoto). 2017. PMID: 28145600
Somatic mosaic deletions involving SCN1A cause Dravet syndrome.
Nakayama T, Ishii A, Yoshida T, Nasu H, Shimojima K, Yamamoto T, Kure S, Hirose S. Nakayama T, et al. Among authors: shimojima k. Am J Med Genet A. 2018 Mar;176(3):657-662. doi: 10.1002/ajmg.a.38596. Epub 2018 Jan 17. Am J Med Genet A. 2018. PMID: 29341473
Tatton-Brown-Rahman syndrome due to 2p23 microdeletion.
Okamoto N, Toribe Y, Shimojima K, Yamamoto T. Okamoto N, et al. Among authors: shimojima k. Am J Med Genet A. 2016 May;170A(5):1339-42. doi: 10.1002/ajmg.a.37588. Epub 2016 Feb 11. Am J Med Genet A. 2016. PMID: 26866722
140 results