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

Year Number of Results
2002 1
2003 1
2004 4
2005 8
2006 6
2007 4
2008 3
2009 13
2010 6
2011 7
2012 9
2013 11
2014 12
2015 14
2016 14
2017 7
2018 6
2019 6
2020 12
2021 5
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129 results
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Page 1
Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencing.
Iwama K, Mizuguchi T, Takeshita E, Nakagawa E, Okazaki T, Nomura Y, Iijima Y, Kajiura I, Sugai K, Saito T, Sasaki M, Yuge K, Saikusa T, Okamoto N, Takahashi S, Amamoto M, Tomita I, Kumada S, Anzai Y, Hoshino K, Fattal-Valevski A, Shiroma N, Ohfu M, Moroto M, Tanda K, Nakagawa T, Sakakibara T, Nabatame S, Matsuo M, Yamamoto A, Yukishita S, Inoue K, Waga C, Nakamura Y, Watanabe S, Ohba C, Sengoku T, Fujita A, Mitsuhashi S, Miyatake S, Takata A, Miyake N, Ogata K, Ito S, Saitsu H, Matsuishi T, Goto YI, Matsumoto N. Iwama K, et al. Among authors: yamamoto a. J Med Genet. 2019 Jun;56(6):396-407. doi: 10.1136/jmedgenet-2018-105775. Epub 2019 Mar 6. J Med Genet. 2019. PMID: 30842224
Reply.
Koizumi H, Yamamoto A, Maruko I, Okada AA, Iida T, Kano M, Saito M, Sekiryu T, Kawasaki R. Koizumi H, et al. Among authors: yamamoto a. Am J Ophthalmol. 2016 Aug;168:287-288. doi: 10.1016/j.ajo.2016.05.004. Epub 2016 Jun 2. Am J Ophthalmol. 2016. PMID: 27265886 No abstract available.
Reply.
Okada AA, Yamamoto A, Koizumi H, Kano M, Saito M, Maruko I, Sekiryu T, Iida T. Okada AA, et al. Among authors: yamamoto a. Ophthalmology. 2016 Feb;123(2):e13-e14. doi: 10.1016/j.ophtha.2015.08.032. Ophthalmology. 2016. PMID: 26802715 No abstract available.
Phenotypes of a family with XLH with a novel PHEX mutation.
Yamamoto A, Nakamura T, Ohata Y, Kubota T, Ozono K. Yamamoto A, et al. Hum Genome Var. 2020 Mar 31;7:8. doi: 10.1038/s41439-020-0095-1. eCollection 2020. Hum Genome Var. 2020. PMID: 32257293 Free PMC article.
129 results
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