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

Year Number of Results
1972 1
1973 2
1974 1
1975 2
1977 2
1978 2
1979 2
1980 3
1981 4
1982 3
1983 4
1984 5
1985 2
1986 5
1987 2
1988 8
1989 7
1990 13
1991 18
1992 10
1993 17
1994 16
1995 11
1996 28
1997 15
1998 16
1999 19
2000 20
2001 20
2002 21
2003 17
2004 23
2005 21
2006 22
2007 17
2008 10
2009 8
2010 8
2011 7
2012 9
2013 4
2014 2
2015 1
2016 1
2017 1
2018 1
2019 1
2022 1
2024 0

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419 results

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Page 1
Kabuki syndrome: international consensus diagnostic criteria.
Adam MP, Banka S, Bjornsson HT, Bodamer O, Chudley AE, Harris J, Kawame H, Lanpher BC, Lindsley AW, Merla G, Miyake N, Okamoto N, Stumpel CT, Niikawa N; Kabuki Syndrome Medical Advisory Board. Adam MP, et al. Among authors: niikawa n. J Med Genet. 2019 Feb;56(2):89-95. doi: 10.1136/jmedgenet-2018-105625. Epub 2018 Dec 4. J Med Genet. 2019. PMID: 30514738
Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients.
Niikawa N, Kuroki Y, Kajii T, Matsuura N, Ishikiriyama S, Tonoki H, Ishikawa N, Yamada Y, Fujita M, Umemoto H, et al. Niikawa N, et al. Am J Med Genet. 1988 Nov;31(3):565-89. doi: 10.1002/ajmg.1320310312. Am J Med Genet. 1988. PMID: 3067577 Review.
[Kabuki make-up syndrome].
Miyoshi O, Niikawa N. Miyoshi O, et al. Among authors: niikawa n. Ryoikibetsu Shokogun Shirizu. 1996;(15):317-9. Ryoikibetsu Shokogun Shirizu. 1996. PMID: 9048029 Review. Japanese. No abstract available.
Kabuki make-up syndrome: a review.
Matsumoto N, Niikawa N. Matsumoto N, et al. Among authors: niikawa n. Am J Med Genet C Semin Med Genet. 2003 Feb 15;117C(1):57-65. doi: 10.1002/ajmg.c.10020. Am J Med Genet C Semin Med Genet. 2003. PMID: 12561059 Review.
Molecular basis of Sotos syndrome.
Niikawa N. Niikawa N. Horm Res. 2004;62 Suppl 3:60-5. doi: 10.1159/000080501. Horm Res. 2004. PMID: 15539801 Review.
[Bardet-Biedl syndrome(BBS)].
Yamada K, Niikawa N. Yamada K, et al. Among authors: niikawa n. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):138-9. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057170 Review. Japanese. No abstract available.
13q-/r(13) mosaicism.
Niikawa N, Tamura T, Tomiyasu F, Kajii T. Niikawa N, et al. J Med Genet. 1980 Aug;17(4):316-9. doi: 10.1136/jmg.17.4.316. J Med Genet. 1980. PMID: 7205909 Free PMC article.
9q34.3 deletion syndrome in three unrelated children.
Iwakoshi M, Okamoto N, Harada N, Nakamura T, Yamamori S, Fujita H, Niikawa N, Matsumoto N. Iwakoshi M, et al. Among authors: niikawa n. Am J Med Genet A. 2004 Apr 30;126A(3):278-83. doi: 10.1002/ajmg.a.20602. Am J Med Genet A. 2004. PMID: 15054842 Review.
419 results