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Results by year

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

Year Number of Results
1960 1
1972 1
1974 1
1977 1
1985 1
1987 1
1988 1
1989 2
1990 2
1991 1
1993 2
1995 1
1997 2
1998 5
1999 1
2000 1
2001 8
2002 6
2003 8
2004 7
2005 6
2006 3
2007 8
2008 7
2009 5
2010 3
2011 7
2012 11
2013 14
2014 15
2015 18
2016 11
2017 10
2018 14
2019 11
2020 18
2021 11
2022 4
2023 1
2024 0

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Similar articles for PMID: 14757866

206 results

Results by year

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Page 1
Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1.
Ishihara N, Yamada K, Yamada Y, Miura K, Kato J, Kuwabara N, Hara Y, Kobayashi Y, Hoshino K, Nomura Y, Mimaki M, Ohya K, Matsushima M, Nitta H, Tanaka K, Segawa M, Ohki T, Ezoe T, Kumagai T, Onuma A, Kuroda T, Yoneda M, Yamanaka T, Saeki M, Segawa M, Saji T, Nagaya M, Wakamatsu N. Ishihara N, et al. J Med Genet. 2004 May;41(5):387-93. doi: 10.1136/jmg.2003.016154. J Med Genet. 2004. PMID: 15121779 Free PMC article. No abstract available.
Clinical utility gene card for: Mowat-Wilson syndrome.
Zollino M, Garavelli L, Rauch A. Zollino M, et al. Eur J Hum Genet. 2011 Aug;19(8). doi: 10.1038/ejhg.2011.12. Epub 2011 Feb 23. Eur J Hum Genet. 2011. PMID: 21343952 Free PMC article. No abstract available.
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases.
Wenger TL, Harr M, Ricciardi S, Bhoj E, Santani A, Adam MP, Barnett SS, Ganetzky R, McDonald-McGinn DM, Battaglia D, Bigoni S, Selicorni A, Sorge G, Monica MD, Mari F, Andreucci E, Romano S, Cocchi G, Savasta S, Malbora B, Marangi G, Garavelli L, Zollino M, Zackai EH. Wenger TL, et al. Am J Med Genet A. 2014 Oct;164A(10):2557-66. doi: 10.1002/ajmg.a.36696. Epub 2014 Aug 14. Am J Med Genet A. 2014. PMID: 25123255
The behavioral phenotype of Mowat-Wilson syndrome.
Evans E, Einfeld S, Mowat D, Taffe J, Tonge B, Wilson M. Evans E, et al. Am J Med Genet A. 2012 Feb;158A(2):358-66. doi: 10.1002/ajmg.a.34405. Epub 2012 Jan 13. Am J Med Genet A. 2012. PMID: 22246645
The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.
Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N. Yamada Y, et al. Am J Med Genet A. 2014 Aug;164A(8):1899-908. doi: 10.1002/ajmg.a.36551. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715670
206 results