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

Year Number of Results
2002 2
2007 2
2008 1
2009 1
2013 2
2014 2
2015 2
2016 2
2017 4
2018 1
2019 4
2021 4
2022 5
2023 1
2024 2

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30 results

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Page 1
Oculofaciocardiodental syndrome caused by a novel BCOR variant.
Yamashita T, Hotta J, Jogu Y, Sakai E, Ono C, Bamba H, Suzuki H, Yamada M, Takenouchi T, Kosaki K, Yorifuji T, Hamazaki T, Seto T. Yamashita T, et al. Among authors: seto t. Hum Genome Var. 2023 Jun 12;10(1):18. doi: 10.1038/s41439-023-00244-x. Hum Genome Var. 2023. PMID: 37308473 Free PMC article.
Possible critical region associated with late-onset spasms in 17p13.1-p13.2 microdeletion syndrome: a report of two new cases and review of the literature.
Yamamoto N, Okazaki S, Kuki I, Yamada N, Nagase S, Nukui M, Inoue T, Kawakita R, Yorifuji T, Hoshina T, Seto T, Yamamoto T, Kawawaki H. Yamamoto N, et al. Among authors: seto t. Epileptic Disord. 2022 Jun 1;24(3):567-571. doi: 10.1684/epd.2022.1416. Epileptic Disord. 2022. PMID: 35653098 Review. English.
Effect of Donor NKG2D Polymorphism on Relapse after Haploidentical Transplantation with Post-Transplantation Cyclophosphamide.
Ido K, Koh H, Hirose A, Seto T, Makuuchi Y, Kuno M, Takakuwa T, Okamura H, Nanno S, Nakamae M, Nishimoto M, Nakashima Y, Hino M, Nakamae H. Ido K, et al. Among authors: seto t. Transplant Cell Ther. 2022 Jan;28(1):20.e1-20.e10. doi: 10.1016/j.jtct.2021.09.019. Epub 2021 Oct 1. Transplant Cell Ther. 2022. PMID: 34607074 Free article.
Genome Analysis in Sick Neonates and Infants: High-yield Phenotypes and Contribution of Small Copy Number Variations.
Suzuki H, Nozaki M, Yoshihashi H, Imagawa K, Kajikawa D, Yamada M, Yamaguchi Y, Morisada N, Eguchi M, Ohashi S, Ninomiya S, Seto T, Tokutomi T, Hida M, Toyoshima K, Kondo M, Inui A, Kurosawa K, Kosaki R, Ito Y, Okamoto N, Kosaki K, Takenouchi T. Suzuki H, et al. Among authors: seto t. J Pediatr. 2022 May;244:38-48.e1. doi: 10.1016/j.jpeds.2022.01.033. Epub 2022 Feb 4. J Pediatr. 2022. PMID: 35131284 Free article.
Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders.
Yamamoto T, Imaizumi T, Yamamoto-Shimojima K, Lu Y, Yanagishita T, Shimada S, Chong PF, Kira R, Ueda R, Ishiyama A, Takeshita E, Momosaki K, Ozasa S, Akiyama T, Kobayashi K, Oomatsu H, Kitahara H, Yamaguchi T, Imai K, Kurahashi H, Okumura A, Oguni H, Seto T, Okamoto N. Yamamoto T, et al. Among authors: seto t. Brain Dev. 2019 Oct;41(9):776-782. doi: 10.1016/j.braindev.2019.05.007. Epub 2019 Jun 4. Brain Dev. 2019. PMID: 31171384
Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II.
Kubaski F, Yabe H, Suzuki Y, Seto T, Hamazaki T, Mason RW, Xie L, Onsten TGH, Leistner-Segal S, Giugliani R, Dũng VC, Ngoc CTB, Yamaguchi S, Montaño AM, Orii KE, Fukao T, Shintaku H, Orii T, Tomatsu S. Kubaski F, et al. Among authors: seto t. Biol Blood Marrow Transplant. 2017 Oct;23(10):1795-1803. doi: 10.1016/j.bbmt.2017.06.020. Epub 2017 Jul 1. Biol Blood Marrow Transplant. 2017. PMID: 28673849 Free PMC article.
30 results