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

Year Number of Results
2002 2
2003 3
2005 2
2008 1
2010 1
2015 2
2016 3
2017 1
2018 1
2020 1
2021 0
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17 results
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Page 1
A constitutional jumping translocation involving the Y and acrocentric chromosomes.
Tsutsumi M, Fujita N, Suzuki F, Mishima T, Fujieda S, Watari M, Takahashi N, Tonoki H, Moriwaka O, Endo T, Kurahashi H. Tsutsumi M, et al. Among authors: watari m. Asian J Androl. 2018 Aug 17;21(1):101-3. doi: 10.4103/aja.aja_60_18. Online ahead of print. Asian J Androl. 2018. PMID: 30147084 Free PMC article. No abstract available.
Genetic and prenatal findings in two Japanese patients with Schinzel-Giedion syndrome.
Hishimura N, Watari M, Ohata H, Fuseya N, Wakiguchi S, Tokutomi T, Okuhara K, Takahashi N, Iizuka S, Yamamoto H, Mishima T, Fujieda S, Kobayashi R, Cho K, Kuroda Y, Kurosawa K, Tonoki H. Hishimura N, et al. Among authors: watari m. Clin Case Rep. 2016 Nov 17;5(1):5-8. doi: 10.1002/ccr3.738. eCollection 2017 Jan. Clin Case Rep. 2016. PMID: 28096980 Free PMC article.
Miller-Dieker Syndrome with unbalanced translocation 45, X, psu dic(17;Y)(p13;p11.32) detected by fluorescence in situ hybridization and G-banding analysis using high resolution banding technique.
Mishima T, Watari M, Iwaki Y, Nagai T, Kawamata-Nakamura M, Kobayashi Y, Fujieda S, Oikawa M, Takahashi N, Keira M, Yoshida H, Tonoki H. Mishima T, et al. Among authors: watari m. Congenit Anom (Kyoto). 2017 Mar;57(2):61-63. doi: 10.1111/cga.12193. Congenit Anom (Kyoto). 2017. PMID: 27644460
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