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Journal Abstract Search

173 related items for PubMed ID: 2316963

  • 21. Cerebellar infarction in a patient with Waardenburg syndrome.
    Narod SA, Siegel-Bartelt J, Hoffman HJ.
    Am J Med Genet; 1988 Dec; 31(4):903-7. PubMed ID: 3239580
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  • 22. [Waardenburg syndrome].
    Kemény P, Szentesi A, Votisky P, Marczell M.
    Orv Hetil; 1977 Aug 28; 118(35):2096-9. PubMed ID: 909699
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  • 27. Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.
    Badner JA, Chakravarti A.
    Am J Med Genet; 1990 Jan 28; 35(1):100-4. PubMed ID: 2301458
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  • 30. Waardenburg's syndrome (case reports and review of literature).
    Parekh P, Singh SD, Dulhani JD, Jain NM.
    Indian Pediatr; 1976 Jun 28; 13(6):465-8. PubMed ID: 977116
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  • 31. [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 28; 64(4):194-7. PubMed ID: 4010406
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  • 32. 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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  • 35. Penetrance and variability of major malformation syndromes associated with deafness.
    Pinsky L.
    Birth Defects Orig Artic Ser; 1979 Jan 02; 15(5B):207-26. PubMed ID: 393321
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  • 37. Animal models of pigment and hearing abnormalities in man.
    Brown KS, Bergsma DR, Barrow MV.
    Birth Defects Orig Artic Ser; 1971 Mar 02; 07(4):102-9. PubMed ID: 5173333
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  • 38. [The Waardenburg-Klein syndrome].
    Ortonne JP, Perrot H, Beyvin AJ, Revol L, Thivolet J.
    Ann Dermatol Syphiligr (Paris); 1976 Mar 02; 103(3):245-56. PubMed ID: 1008516
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