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Results by year

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

Year Number of Results
1986 1
1987 1
1988 3
1989 1
1990 2
1991 4
1992 1
1993 1
1994 2
1995 1
1996 1
1997 3
1998 3
1999 7
2000 9
2001 22
2004 1
2005 3
2006 3
2007 1
2008 2
2009 1
2010 2
2011 2
2013 2
2014 3
2015 1
2016 1
2017 3
2018 1
2019 1
2020 4
2021 2
2023 2
2024 0

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Search Results

94 results

Results by year

Filters applied: . Clear all
Page 1
[Melorheostosis].
Tonoki H. Tonoki H. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):165. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528680 Review. Japanese. No abstract available.
[Thanatophoric dysplasia].
Tonoki H. Tonoki H. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):720-1. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528986 Review. Japanese. No abstract available.
[Thanatophoric dysplasia].
Tonoki H. Tonoki H. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):294-5. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057234 Review. Japanese. No abstract available.
[Achondroplasia, hypochondroplasia].
Fujiwara F, Tonoki H. Fujiwara F, et al. Among authors: tonoki h. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):301-3. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057237 Review. Japanese. No abstract available.
[Tonoki syndrome].
Tonoki H. Tonoki H. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):734-5. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528994 Review. Japanese. No abstract available.
[Megalencephaly].
Tonoki H. Tonoki H. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):160-1. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528677 Review. Japanese. No abstract available.
[Meningomyelocele].
Tonoki H. Tonoki H. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):168-9. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528683 Review. Japanese. No abstract available.
[Meningocele].
Tonoki H. Tonoki H. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):166. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528681 Review. Japanese. No abstract available.
A Noonan-like pediatric patient with a de novo CBL pathogenic variant and an RNF213 polymorphism p.R4810K presenting with cardiopulmonary arrest due to left main coronary artery ostial atresia.
Chida-Nagai A, Tonoki H, Makita N, Ishiyama H, Ihara M, Maruo Y, Tsujioka T, Sasaki D, Izumi G, Yamazawa H, Kato N, Ito M, Fujimura M, Sasaki O, Takeda A. Chida-Nagai A, et al. Among authors: tonoki h. Am J Med Genet A. 2023 Dec;191(12):2837-2842. doi: 10.1002/ajmg.a.63370. Epub 2023 Aug 9. Am J Med Genet A. 2023. PMID: 37554039
94 results