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Journal Abstract Search

139 related items for PubMed ID: 1952586

  • 1. Hearing impairment and pigmentary disturbance.
    Beighton P, Ramesar R, Winship I, Viljoen D, Greenberg J, Young K, Curtis D, Sellars S.
    Ann N Y Acad Sci; 1991; 630():152-66. PubMed ID: 1952586
    [Abstract] [Full Text] [Related]

  • 2. Spontaneous contraction of leukodermic patches in Waardenburg syndrome.
    Chang T, Hashimoto K, Bawle EV.
    J Dermatol; 1993 Nov; 20(11):707-11. PubMed ID: 8300941
    [Abstract] [Full Text] [Related]

  • 3. [Heterochromia iridis, congenital deafness and skin pigmentary abnormalities: Waardenburg syndrome].
    Jiménez Gómez N, Ballester Martínez MA, Urrutia Hernando S, Jaén Olasolo P.
    Med Clin (Barc); 2014 Mar 20; 142(6):e11. PubMed ID: 24029453
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. The Waardenburg syndrome in deaf children in southern Africa.
    Sellars S, Beighton P.
    S Afr Med J; 1983 May 07; 63(19):725-8. PubMed ID: 6845084
    [Abstract] [Full Text] [Related]

  • 6. Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA).
    Morell R, Spritz RA, Ho L, Pierpont J, Guo W, Friedman TB, Asher JH.
    Hum Mol Genet; 1997 May 07; 6(5):659-64. PubMed ID: 9158138
    [Abstract] [Full Text] [Related]

  • 7. Piebaldism: an autonomous autosomal dominant entity.
    Winship I, Young K, Martell R, Ramesar R, Curtis D, Beighton P.
    Clin Genet; 1991 May 07; 39(5):330-7. PubMed ID: 1860249
    [Abstract] [Full Text] [Related]

  • 8. Phenotypic discriminants in the Waardenburg syndrome.
    Winship I, Beighton P.
    Clin Genet; 1992 Apr 07; 41(4):181-8. PubMed ID: 1576755
    [Abstract] [Full Text] [Related]

  • 9. 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 07; 7(1):17-20. PubMed ID: 9546825
    [Abstract] [Full Text] [Related]

  • 10. Heterogeneity in Waardenburg syndrome.
    Hageman MJ, Delleman JW.
    Am J Hum Genet; 1977 Sep 07; 29(5):468-85. PubMed ID: 331943
    [Abstract] [Full Text] [Related]

  • 11. Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism.
    Gironi LC, Colombo E, Brusco A, Grosso E, Naretto VG, Guala A, Di Gregorio E, Zonta A, Zottarelli F, Pasini B, Savoia P.
    Medicina (Kaunas); 2019 Jul 07; 55(7):. PubMed ID: 31284637
    [Abstract] [Full Text] [Related]

  • 12. Hereditary childhood hearing loss and integumentary system disease.
    Konigsmark BW.
    J Pediatr; 1972 Jun 07; 80(6):909-19. PubMed ID: 5026034
    [No Abstract] [Full Text] [Related]

  • 13. Piebaldism, Waardenburg syndrome, and related disorders of melanocyte development.
    Spritz RA.
    Semin Cutan Med Surg; 1997 Mar 07; 16(1):15-23. PubMed ID: 9125761
    [Abstract] [Full Text] [Related]

  • 14. A coloured family showing features of Waardenburg's syndrome.
    Rappoport AS.
    S Afr Med J; 1970 Apr 04; 44(14):412-3. PubMed ID: 5443890
    [No Abstract] [Full Text] [Related]

  • 15. The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1).
    Morell R, Friedman TB, Asher JH, Robbins LG.
    J Med Genet; 1997 Jun 04; 34(6):447-52. PubMed ID: 9192262
    [Abstract] [Full Text] [Related]

  • 16. Double heterozygous mutations of MITF and PAX3 result in Waardenburg syndrome with increased penetrance in pigmentary defects.
    Yang T, Li X, Huang Q, Li L, Chai Y, Sun L, Wang X, Zhu Y, Wang Z, Huang Z, Li Y, Wu H.
    Clin Genet; 2013 Jan 04; 83(1):78-82. PubMed ID: 22320238
    [Abstract] [Full Text] [Related]

  • 17. Hereditary congenital severe deafness syndromes.
    Konigsmark BW.
    Ann Otol Rhinol Laryngol; 1971 Apr 04; 80(2):269-88. PubMed ID: 4927796
    [No Abstract] [Full Text] [Related]

  • 18. Pigmentary anomalies and hearing loss.
    Toriello HV.
    Adv Otorhinolaryngol; 2011 Apr 04; 70():50-55. PubMed ID: 21358185
    [Abstract] [Full Text] [Related]

  • 19. [The Waardenburg-Klein syndrome].
    ARNVIG J.
    Nord Med; 1960 Jul 28; 64():953-5. PubMed ID: 13794441
    [No Abstract] [Full Text] [Related]

  • 20. Waardenburg syndrome in the Turkish deaf population.
    Silan F, Zafer C, Onder I.
    Genet Couns; 2006 Jul 28; 17(1):41-8. PubMed ID: 16719276
    [Abstract] [Full Text] [Related]

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