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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

64 related articles for article (PubMed ID: 37221585)

  • 21. Great clinical variability of Nance Horan syndrome due to deleterious
    Hernández V; Pascual-Camps I; Aparisi MJ; Martínez-Matilla M; Martínez F; Cerón JA; Pedrola L
    Ophthalmic Genet; 2019 Dec; 40(6):553-557. PubMed ID: 31755796
    [No Abstract]   [Full Text] [Related]  

  • 22. Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders.
    de La Dure-Molla M; Fournier BP; Manzanares MC; Acevedo AC; Hennekam RC; Friedlander L; Boy-Lefèvre ML; Kerner S; Toupenay S; Garrec P; Vi-Fane B; Felizardo R; Berteretche MV; Jordan L; Ferré F; Clauss F; Jung S; de Chalendar M; Troester S; Kawczynski M; Chaloyard J; ; Manière MC; Berdal A; Bloch-Zupan A
    Am J Med Genet A; 2019 Oct; 179(10):1913-1981. PubMed ID: 31468724
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families.
    Güven Y; Bal E; Altunoglu U; Yücel E; Hadj-Rabia S; Koruyucu M; Bahar Tuna E; Çıldır Ş; Aktören O; Bodemer C; Uyguner ZO; Smahi A; Kayserili H
    Cytogenet Genome Res; 2019; 157(4):189-196. PubMed ID: 30974434
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. Nance-Horan Syndrome: A Rare Case Report.
    Sharma S; Datta P; Sabharwal JR; Datta S
    Contemp Clin Dent; 2017; 8(3):469-472. PubMed ID: 29042737
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.
    Messina-Baas O; Cuevas-Covarrubias SA
    Mol Syndromol; 2017 Mar; 8(2):58-78. PubMed ID: 28611546
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Nance-Horan syndrome-The oral perspective on a rare disease.
    Gjørup H; Haubek D; Jacobsen P; Ostergaard JR
    Am J Med Genet A; 2017 Jan; 173(1):88-98. PubMed ID: 27616609
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetics of Congenital Cataract.
    Pichi F; Lembo A; Serafino M; Nucci P
    Dev Ophthalmol; 2016; 57():1-14. PubMed ID: 27043388
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Dental Stigmata of Congenital Syphilis: A Historic Review With Present Day Relevance.
    Nissanka-Jayasuriya EH; Odell EW; Phillips C
    Head Neck Pathol; 2016 Sep; 10(3):327-31. PubMed ID: 26897633
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. A possible cranio-oro-facial phenotype in Cockayne syndrome.
    Bloch-Zupan A; Rousseaux M; Laugel V; Schmittbuhl M; Mathis R; Desforges E; Koob M; Zaloszyc A; Dollfus H; Laugel V
    Orphanet J Rare Dis; 2013 Jan; 8():9. PubMed ID: 23311583
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Phenotype-genotype correlation in potential female carriers of X-linked developmental cataract (Nance-Horan syndrome).
    Khan AO; Aldahmesh MA; Mohamed JY; Alkuraya FS
    Ophthalmic Genet; 2012 Jun; 33(2):89-95. PubMed ID: 22229851
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genes.
    Van Esch H; Jansen A; Bauters M; Froyen G; Fryns JP
    Am J Med Genet A; 2007 Feb; 143(4):364-9. PubMed ID: 17256798
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Kabuki syndrome: oral and general features seen in a 2-year-old Chinese boy.
    Atar M; Lee W; O'Donnell D
    Int J Paediatr Dent; 2006 May; 16(3):222-6. PubMed ID: 16643546
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 4.