These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
150 related articles for article (PubMed ID: 17417607)
1. Identification of three novel NHS mutations in families with Nance-Horan syndrome. Huang KM; Wu J; Brooks SP; Hardcastle AJ; Lewis RA; Stambolian D Mol Vis; 2007 Mar; 13():470-4. PubMed ID: 17417607 [TBL] [Abstract][Full Text] [Related]
2. Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing. Hong N; Chen YH; Xie C; Xu BS; Huang H; Li X; Yang YQ; Huang YP; Deng JL; Qi M; Gu YS J Zhejiang Univ Sci B; 2014 Aug; 15(8):727-34. PubMed ID: 25091991 [TBL] [Abstract][Full Text] [Related]
3. [Clinical and genetic characterization of three families with Nance-Horan syndrome caused by NHS gene mutations]. Li L; Zheng GY; Song JX; Yue JF; Tan N Zhonghua Yan Ke Za Zhi; 2024 Sep; 60(9):757-765. PubMed ID: 39267554 [No Abstract] [Full Text] [Related]
4. A novel Xp22.13 microdeletion in Nance-Horan syndrome. Accogli A; Traverso M; Madia F; Bellini T; Vari MS; Pinto F; Capra V Birth Defects Res; 2017 Jul; 109(11):866-868. PubMed ID: 28464487 [TBL] [Abstract][Full Text] [Related]
5. Identification of a novel NHS mutation in a Chinese family with Nance-Horan syndrome. Li A; Li B; Wu L; Yang L; Chen N; Ma Z Curr Eye Res; 2015 Apr; 40(4):434-8. PubMed ID: 25266737 [TBL] [Abstract][Full Text] [Related]
6. A novel NHS mutation causes Nance-Horan Syndrome in a Chinese family. Tian Q; Li Y; Kousar R; Guo H; Peng F; Zheng Y; Yang X; Long Z; Tian R; Xia K; Lin H; Pan Q BMC Med Genet; 2017 Jan; 18(1):2. PubMed ID: 28061824 [TBL] [Abstract][Full Text] [Related]
7. A Turkish family with Nance-Horan Syndrome due to a novel mutation. Tug E; Dilek NF; Javadiyan S; Burdon KP; Percin FE Gene; 2013 Aug; 525(1):141-5. PubMed ID: 23566852 [TBL] [Abstract][Full Text] [Related]
9. A novel small deletion in the NHS gene associated with Nance-Horan syndrome. Li H; Yang L; Sun Z; Yuan Z; Wu S; Sui R Sci Rep; 2018 Feb; 8(1):2398. PubMed ID: 29402928 [TBL] [Abstract][Full Text] [Related]
10. Congenital diaphragmatic hernia as a part of Nance-Horan syndrome? Kammoun M; Brady P; De Catte L; Deprest J; Devriendt K; Vermeesch JR Eur J Hum Genet; 2018 Mar; 26(3):359-366. PubMed ID: 29358614 [TBL] [Abstract][Full Text] [Related]
11. Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature. Gómez-Laguna L; Martínez-Herrera A; Reyes-de la Rosa ADP; García-Delgado C; Nieto-Martínez K; Fernández-Ramírez F; Valderrama-Atayupanqui TY; Morales-Jiménez AB; Villa-Morales J; Kofman S; Cervantes A; Morán-Barroso VF Ophthalmic Genet; 2018; 39(1):56-62. PubMed ID: 28922055 [TBL] [Abstract][Full Text] [Related]
12. Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome. Ling C; Sui R; Yao F; Wu Z; Zhang X; Zhang S BMC Med Genet; 2019 Jan; 20(1):14. PubMed ID: 30642278 [TBL] [Abstract][Full Text] [Related]
13. Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation. Burdon KP; McKay JD; Sale MM; Russell-Eggitt IM; Mackey DA; Wirth MG; Elder JE; Nicoll A; Clarke MP; FitzGerald LM; Stankovich JM; Shaw MA; Sharma S; Gajovic S; Gruss P; Ross S; Thomas P; Voss AK; Thomas T; Gécz J; Craig JE Am J Hum Genet; 2003 Nov; 73(5):1120-30. PubMed ID: 14564667 [TBL] [Abstract][Full Text] [Related]
14. Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family. Ramprasad VL; Thool A; Murugan S; Nancarrow D; Vyas P; Rao SK; Vidhya A; Ravishankar K; Kumaramanickavel G Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):17-23. PubMed ID: 15623749 [TBL] [Abstract][Full Text] [Related]
15. The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly. Chograni M; Rejeb I; Jemaa LB; Châabouni M; Bouhamed HC Eur J Hum Genet; 2011 Aug; 19(8):851-6. PubMed ID: 21559051 [TBL] [Abstract][Full Text] [Related]
16. Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome. Liao HM; Niu DM; Chen YJ; Fang JS; Chen SJ; Chen CH J Hum Genet; 2011 Jan; 56(1):8-11. PubMed ID: 20882036 [TBL] [Abstract][Full Text] [Related]
17. X-linked cataract and Nance-Horan syndrome are allelic disorders. Coccia M; Brooks SP; Webb TR; Christodoulou K; Wozniak IO; Murday V; Balicki M; Yee HA; Wangensteen T; Riise R; Saggar AK; Park SM; Kanuga N; Francis PJ; Maher ER; Moore AT; Russell-Eggitt IM; Hardcastle AJ Hum Mol Genet; 2009 Jul; 18(14):2643-55. PubMed ID: 19414485 [TBL] [Abstract][Full Text] [Related]
18. Identification of the gene for Nance-Horan syndrome (NHS). Brooks SP; Ebenezer ND; Poopalasundaram S; Lehmann OJ; Moore AT; Hardcastle AJ J Med Genet; 2004 Oct; 41(10):768-71. PubMed ID: 15466011 [TBL] [Abstract][Full Text] [Related]