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Results by year

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

Year Number of Results
1979 2
1983 2
1984 1
1988 6
1989 5
1990 1
1991 3
1992 3
1993 3
1994 1
1995 1
1996 2
1997 5
1998 3
1999 2
2000 4
2001 20
2002 2
2003 2
2004 1
2005 2
2006 5
2007 3
2008 2
2009 2
2011 1
2012 5
2013 5
2014 4
2015 1
2017 1
2018 1
2019 2
2020 2
2022 1
2023 1
2024 0

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Article type

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Search Results

103 results

Results by year

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Page 1
[Aicardi syndrome].
Naritomi K. Naritomi K. Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):118-21. Ryoikibetsu Shokogun Shirizu. 2002. PMID: 12483842 Review. Japanese. No abstract available.
[Osteoglophonic dysplasia].
Naritomi K. Naritomi K. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):420-1. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528815 Review. Japanese. No abstract available.
[Osteolysis].
Naritomi K. Naritomi K. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):422-3. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528816 Review. Japanese. No abstract available.
[Osteoectasia].
Naritomi K. Naritomi K. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):414-5. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528811 Review. Japanese. No abstract available.
[Osteodysplasty].
Naritomi K. Naritomi K. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):409-11. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528809 Review. Japanese. No abstract available.
[Osteomesopyknosis].
Naritomi K. Naritomi K. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):424-5. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528817 Review. Japanese. No abstract available.
[Optico-cochleo-dentate-degeneration].
Naritomi K. Naritomi K. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):388-9. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528799 Review. Japanese. No abstract available.
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.
Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LC, Eussen BH, Van Hemel JO, Lozzio C, Schwartz S, Dowhanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D. Warburton PE, et al. Among authors: naritomi k. Am J Hum Genet. 2000 Jun;66(6):1794-806. doi: 10.1086/302924. Epub 2000 Apr 24. Am J Hum Genet. 2000. PMID: 10777715 Free PMC article. Review.
Clinical correlations of mutations affecting six components of the SWI/SNF complex: detailed description of 21 patients and a review of the literature.
Kosho T, Okamoto N, Ohashi H, Tsurusaki Y, Imai Y, Hibi-Ko Y, Kawame H, Homma T, Tanabe S, Kato M, Hiraki Y, Yamagata T, Yano S, Sakazume S, Ishii T, Nagai T, Ohta T, Niikawa N, Mizuno S, Kaname T, Naritomi K, Narumi Y, Wakui K, Fukushima Y, Miyatake S, Mizuguchi T, Saitsu H, Miyake N, Matsumoto N. Kosho T, et al. Among authors: naritomi k. Am J Med Genet A. 2013 Jun;161A(6):1221-37. doi: 10.1002/ajmg.a.35933. Epub 2013 May 1. Am J Med Genet A. 2013. PMID: 23637025 Review.
103 results