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Journal Abstract Search

149 related items for PubMed ID: 6463802

  • 1. Waardenburg syndrome in South Africa. Part I. An evaluation of the clinical findings in 11 families.
    de Saxe M, Kromberg JG, Jenkins T.
    S Afr Med J; 1984 Aug 18; 66(7):256-61. PubMed ID: 6463802
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  • 2. Waardenburg syndrome in South Africa. Part II. Is there founder effect for type I?
    de Saxe M, Kromberg JG, Jenkins T.
    S Afr Med J; 1984 Aug 25; 66(8):291-3. PubMed ID: 6474292
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  • 5. Spontaneous contraction of leukodermic patches in Waardenburg syndrome.
    Chang T, Hashimoto K, Bawle EV.
    J Dermatol; 1993 Nov 25; 20(11):707-11. PubMed ID: 8300941
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  • 7. Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature.
    Baldwin CT, Hoth CF, Macina RA, Milunsky A.
    Am J Med Genet; 1995 Aug 28; 58(2):115-22. PubMed ID: 8533800
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  • 9. Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations.
    Jalilian N, Tabatabaiefar MA, Farhadi M, Bahrami T, Emamdjomeh H, Noori-Daloii MR.
    Gene; 2015 Dec 15; 574(2):302-7. PubMed ID: 26275939
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  • 10. [Families with recurrent cases of Waardenburg-Klein syndrome].
    Bliumina MG, Moskovkina AG.
    Genetika; 1985 Jun 15; 21(6):1062-5. PubMed ID: 4029612
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  • 12. 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
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  • 13. 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 02; 34(6):447-52. PubMed ID: 9192262
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  • 14. Apparent non-penetrance for dystopia in Waardenburg syndrome type I, with some hints on the diagnosis of dystopia canthorum.
    Arias S, Mota M.
    J Genet Hum; 1978 Jun 02; 26(2):103-31. PubMed ID: 670940
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  • 16. Waardenburg syndrome.
    Read AP, Newton VE.
    J Med Genet; 1997 Aug 02; 34(8):656-65. PubMed ID: 9279758
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  • 20. Upper limb involvement in the Klein-Waardenburg syndrome.
    Goodman RM, Lewithal I, Solomon A, Klein D.
    Am J Med Genet; 1982 Apr 02; 11(4):425-33. PubMed ID: 7091186
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