Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

141 results

Results by year

Filters applied: . Clear all
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
9q22 Deletion--first familial case.
Siggberg L, Peippo M, Sipponen M, Miikkulainen T, Shimojima K, Yamamoto T, Ignatius J, Knuutila S. Siggberg L, et al. Among authors: shimojima k. Orphanet J Rare Dis. 2011 Jun 22;6:45. doi: 10.1186/1750-1172-6-45. Orphanet J Rare Dis. 2011. PMID: 21693067 Free PMC article.
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
MECP2 duplication syndrome in both genders.
Shimada S, Okamoto N, Ito M, Arai Y, Momosaki K, Togawa M, Maegaki Y, Sugawara M, Shimojima K, Osawa M, Yamamoto T. Shimada S, et al. Among authors: shimojima k. Brain Dev. 2013 May;35(5):411-9. doi: 10.1016/j.braindev.2012.07.010. Epub 2012 Aug 9. Brain Dev. 2013. PMID: 22877836
141 results