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 *

79 related articles for article (PubMed ID: 22555841)

  • 1. [Waardenburg Syndrome: a review of literature and case reports].
    Salvatore S; Carnevale C; Infussi R; Arrico L; Mafrici M; Plateroti AM; Vingolo EM
    Clin Ter; 2012; 163(2):e85-94. PubMed ID: 22555841
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Waardenburg syndrome.
    Konno P; Silm H
    J Eur Acad Dermatol Venereol; 2001 Jul; 15(4):330-3. PubMed ID: 11730045
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Review and update of mutations causing Waardenburg syndrome.
    Pingault V; Ente D; Dastot-Le Moal F; Goossens M; Marlin S; Bondurand N
    Hum Mutat; 2010 Apr; 31(4):391-406. PubMed ID: 20127975
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Waardenburg syndrome type 1.
    Karaman A; Aliagaoglu C
    Dermatol Online J; 2006 Mar; 12(3):21. PubMed ID: 16638435
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Waardenburg syndrome: a report of three cases.
    Ghosh SK; Bandyopadhyay D; Ghosh A; Biswas SK; Mandal RK
    Indian J Dermatol Venereol Leprol; 2010; 76(5):550-2. PubMed ID: 20826997
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.
    Liu XZ; Newton VE; Read AP
    Am J Med Genet; 1995 Jan; 55(1):95-100. PubMed ID: 7702105
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Waardenburg syndrome Type II.
    Singh I; Maharjan M; Gautam DK; Mehar R; Gathwala G
    Kathmandu Univ Med J (KUMJ); 2006; 4(4):506-9. PubMed ID: 18603964
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Shah-Waardenburg syndrome.
    Sankar R
    Dermatol Online J; 2008 Jan; 14(1):19. PubMed ID: 18319036
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Waardenburg syndrome in the Turkish deaf population.
    Silan F; Zafer C; Onder I
    Genet Couns; 2006; 17(1):41-8. PubMed ID: 16719276
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic discriminants in the Waardenburg syndrome.
    Winship I; Beighton P
    Clin Genet; 1992 Apr; 41(4):181-8. PubMed ID: 1576755
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Audiometric findings in Waardenburg's syndrome amongst the institutionalised deaf/blind in Kaduna-Nigeria.
    Ahmed AO; Samaila E; Abah ER; Oladigbolu KK; Merali H; Abubakar A
    Niger J Med; 2011; 20(1):28-32. PubMed ID: 21970256
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Waardenburg syndrome associated with laryngomalacia.
    Thapa R; Mallick D; Ghosh A; Ghosh A
    Singapore Med J; 2009 Dec; 50(12):e401-3. PubMed ID: 20087539
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Waardenburg's syndrome].
    Cacheux V; Delezoide AL; Vekemans M
    C R Seances Soc Biol Fil; 1996; 190(5-6):577-80. PubMed ID: 9074723
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Waardenburg's syndrome.
    Parsons G; Mokela D
    P N G Med J; 1993 Dec; 36(4):353. PubMed ID: 7941767
    [No Abstract]   [Full Text] [Related]  

  • 15. [A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC].
    Bassabi SK; Medji AP; Doutetien C; Oussa G; Hounkpe YY; Vodouhe SJ; Babagbeto M; Latoundji S
    J Fr Ophtalmol; 1997; 20(5):387-90. PubMed ID: 9238477
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Waardenburg syndrome].
    Veres G; Kárpáti S; Karászi V; Czenthe Z; Horváth A
    Orv Hetil; 2004 Jul; 145(29):1523-6. PubMed ID: 15453024
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification and functional analysis of SOX10 missense mutations in different subtypes of Waardenburg syndrome.
    Chaoui A; Watanabe Y; Touraine R; Baral V; Goossens M; Pingault V; Bondurand N
    Hum Mutat; 2011 Dec; 32(12):1436-49. PubMed ID: 21898658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.
    Hughes AE; Newton VE; Liu XZ; Read AP
    Nat Genet; 1994 Aug; 7(4):509-12. PubMed ID: 7951321
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Klein-Waardenburg syndrome. Report of 3 cases in a family with a review of the literature].
    Piechowiak H; Wasmer C; Göbel FD
    Laryngol Rhinol Otol (Stuttg); 1985 Apr; 64(4):194-7. PubMed ID: 4010406
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Open angle glaucoma as a manifestation of Waardenburg's syndrome.
    Gupta V; Aggarwal HC
    Indian J Ophthalmol; 2000 Mar; 48(1):49-50. PubMed ID: 11271935
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.