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Journal Abstract Search

85 related items for PubMed ID: 1481835

  • 21. [Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)].
    Meinecke P.
    Klin Padiatr; 1982 Mar; 194(2):112-6. PubMed ID: 7098370
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  • 22. [Waardenburg syndrome].
    Veres G, Kárpáti S, Karászi V, Czenthe Z, Horváth A.
    Orv Hetil; 2004 Jul 18; 145(29):1523-6. PubMed ID: 15453024
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  • 23. [Atypical manifestations in familial type 1 Waardenburg syndrome].
    Sans B, Calvas P, Bazex J.
    Ann Dermatol Venereol; 1998 Jan 18; 125(1):37-41. PubMed ID: 9747206
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  • 27. [Waardenburg's syndrome].
    Gimñenez F, Carbonell R, Pérez F, Lozano I.
    An Otorrinolaringol Ibero Am; 1994 Jan 18; 21(4):425-32. PubMed ID: 8092450
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  • 28. [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 18; 64(4):194-7. PubMed ID: 4010406
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  • 29. [Waardenburg's syndrome. A familial case relating to 4 generations and 23 individuals].
    Roux C, Baheux G, Gaulier M, Caldera R, Soepardan L.
    Ann Genet; 1970 Jun 18; 13(2):125-8. PubMed ID: 5310696
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  • 33. Fetus with unbalanced translocation involving chromosomes 2 and 11.
    Norman AM, Read AP, Clark A, Haslam J, Donnai D.
    Clin Dysmorphol; 1992 Jan 18; 1(1):53-6. PubMed ID: 1342860
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  • 35. Genetic heterogeneity in the Waardenburg syndrome.
    Arias S.
    Birth Defects Orig Artic Ser; 1971 Mar 18; 07(4):87-101. PubMed ID: 5006208
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  • 39. [Make a diagnosis. Waardenburg's syndrome type 1].
    Aksu F.
    Padiatr Padol; 1983 Mar 18; 18(4):399-402. PubMed ID: 6646790
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  • 40. Waardenburg syndrome Type II.
    Singh I, Maharjan M, Gautam DK, Mehar R, Gathwala G.
    Kathmandu Univ Med J (KUMJ); 2006 Mar 18; 4(4):506-9. PubMed ID: 18603964
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