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Journal Abstract Search

302 related items for PubMed ID: 16719276

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

  • 2. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.
    Liu XZ, Newton VE, Read AP.
    Am J Med Genet; 1995 Jan 02; 55(1):95-100. PubMed ID: 7702105
    [Abstract] [Full Text] [Related]

  • 3. 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 Jan 02; 20(1):28-32. PubMed ID: 21970256
    [Abstract] [Full Text] [Related]

  • 4. Waardenburg's syndrome in Kenyan Africans.
    Hageman MJ.
    Trop Geogr Med; 1978 Mar 02; 30(1):45-55. PubMed ID: 675827
    [Abstract] [Full Text] [Related]

  • 5. Waardenburg syndrome type 1.
    Karaman A, Aliagaoglu C.
    Dermatol Online J; 2006 Mar 30; 12(3):21. PubMed ID: 16638435
    [Abstract] [Full Text] [Related]

  • 6. [Hereditary unilateral deaf-mutism as a variable manifestation of bilateral deaf-mutism or hearing loss].
    Graf K.
    Laryngorhinootologie; 1992 May 30; 71(5):242-5. PubMed ID: 1616543
    [Abstract] [Full Text] [Related]

  • 7. Phenotypic discriminants in the Waardenburg syndrome.
    Winship I, Beighton P.
    Clin Genet; 1992 Apr 30; 41(4):181-8. PubMed ID: 1576755
    [Abstract] [Full Text] [Related]

  • 8. Waardenburg syndrome.
    Konno P, Silm H.
    J Eur Acad Dermatol Venereol; 2001 Jul 30; 15(4):330-3. PubMed ID: 11730045
    [Abstract] [Full Text] [Related]

  • 9. Cerebellar infarction in a patient with Waardenburg syndrome.
    Narod SA, Siegel-Bartelt J, Hoffman HJ.
    Am J Med Genet; 1988 Dec 30; 31(4):903-7. PubMed ID: 3239580
    [Abstract] [Full Text] [Related]

  • 10. [Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)].
    Meinecke P.
    Klin Padiatr; 1982 Mar 30; 194(2):112-6. PubMed ID: 7098370
    [Abstract] [Full Text] [Related]

  • 11. Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome).
    Edery P, Attié T, Amiel J, Pelet A, Eng C, Hofstra RM, Martelli H, Bidaud C, Munnich A, Lyonnet S.
    Nat Genet; 1996 Apr 30; 12(4):442-4. PubMed ID: 8630502
    [Abstract] [Full Text] [Related]

  • 12. [Waardenburg's syndrome (type II) in 2 children, without parental involvement: genetic counseling].
    Dodinval P, Lhussier-Grodos TM.
    J Genet Hum; 1981 Sep 30; 29(3):273-84. PubMed ID: 7334349
    [No Abstract] [Full Text] [Related]

  • 13. Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.
    Badner JA, Chakravarti A.
    Am J Med Genet; 1990 Jan 30; 35(1):100-4. PubMed ID: 2301458
    [Abstract] [Full Text] [Related]

  • 14. [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 Jan 30; 20(5):387-90. PubMed ID: 9238477
    [Abstract] [Full Text] [Related]

  • 15. Waardenburg syndrome: a report of three cases.
    Ghosh SK, Bandyopadhyay D, Ghosh A, Biswas SK, Mandal RK.
    Indian J Dermatol Venereol Leprol; 2010 Jan 30; 76(5):550-2. PubMed ID: 20826997
    [Abstract] [Full Text] [Related]

  • 16. Waardenburg syndrome associated with laryngomalacia.
    Thapa R, Mallick D, Ghosh A, Ghosh A.
    Singapore Med J; 2009 Dec 30; 50(12):e401-3. PubMed ID: 20087539
    [Abstract] [Full Text] [Related]

  • 17. Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome).
    Amiel J, Watkin PM, Tassabehji M, Read AP, Winter RM.
    Clin Dysmorphol; 1998 Jan 30; 7(1):17-20. PubMed ID: 9546825
    [Abstract] [Full Text] [Related]

  • 18. Cochlear implantation in Waardenburg's syndrome.
    Migirov L, Henkin Y, Hildesheimer M, Muchnik C, Kronenberg J.
    Acta Otolaryngol; 2005 Jul 30; 125(7):713-7. PubMed ID: 16012032
    [Abstract] [Full Text] [Related]

  • 19. Shah-Waardenburg syndrome.
    Sankar R.
    Dermatol Online J; 2008 Jan 15; 14(1):19. PubMed ID: 18319036
    [Abstract] [Full Text] [Related]

  • 20. [Make a diagnosis. Waardenburg's syndrome type 1].
    Aksu F.
    Padiatr Padol; 1983 Jan 15; 18(4):399-402. PubMed ID: 6646790
    [No Abstract] [Full Text] [Related]

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