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Results by year

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

Year Number of Results
1993 88
1997 2
1998 1
1999 2
2000 4
2001 5
2002 5
2003 7
2004 6
2005 5
2006 5
2007 8
2008 6
2009 7
2010 2
2011 2
2013 3
2014 3
2015 2
2016 6
2017 5
2018 4
2019 10
2020 11
2021 13
2022 26
2023 20
2024 6

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Similar articles for PMID: 20301770

101 results

Results by year

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Page 1
Feingold Syndrome 1.
Marcelis CLM, de Brouwer APM. Marcelis CLM, et al. 2009 Jun 30 [updated 2019 Apr 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2009 Jun 30 [updated 2019 Apr 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301770 Free Books & Documents. Review.
Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.
Tedesco MG, Lonardo F, Ceccarini C, Cesarano C, Digilio MC, Magliozzi M, Rogaia D, Mencarelli A, Leoni C, Piscopo C, Imperatore V, Falco MT, Fontana P, Nardone AM, Novelli A, Troiani S, Seri M, Prontera P. Tedesco MG, et al. Am J Med Genet A. 2021 Apr;185(4):1204-1210. doi: 10.1002/ajmg.a.62068. Epub 2021 Jan 14. Am J Med Genet A. 2021. PMID: 33442900
A new variant of MYCN gene as a cause of Feingold syndrome.
Zeka N, Bejiqi R, Gerguri A, Zogaj L, Jashari H. Zeka N, et al. Clin Case Rep. 2022 May 23;10(5):e05886. doi: 10.1002/ccr3.5886. eCollection 2022 May. Clin Case Rep. 2022. PMID: 35620261 Free PMC article.
Noonan Syndrome.
Roberts AE. Roberts AE. 2001 Nov 15 [updated 2022 Feb 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2001 Nov 15 [updated 2022 Feb 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301303 Free Books & Documents. Review.
Oral-Facial-Digital Syndrome Type I.
Franco B, Bruel AL, Thauvin-Robinet C. Franco B, et al. 2002 Jul 24 [updated 2023 May 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2002 Jul 24 [updated 2023 May 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301367 Free Books & Documents. Review.
Kabuki Syndrome.
Adam MP, Hudgins L, Hannibal M. Adam MP, et al. 2011 Sep 1 [updated 2024 Apr 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2011 Sep 1 [updated 2024 Apr 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 21882399 Free Books & Documents. Review.
[Feingold syndrome].
Alessandri JL, Graber D, Tiran-Rajaofera I, Montbrun A, Pilorget H, Samperiz S, Attali T, de Napoli-Cocci S. Alessandri JL, et al. Arch Pediatr. 2000 Jun;7(6):637-40. doi: 10.1016/s0929-693x(00)80132-3. Arch Pediatr. 2000. PMID: 10911531 French.
101 results