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Journal Abstract Search

141 related items for PubMed ID: 7098370

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  • 8. Waardenburg syndrome: a report of three cases.
    Ghosh SK, Bandyopadhyay D, Ghosh A, Biswas SK, Mandal RK.
    Indian J Dermatol Venereol Leprol; 2010; 76(5):550-2. PubMed ID: 20826997
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  • 9. Genetic heterogeneity in the Waardenburg syndrome.
    Arias S.
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):87-101. PubMed ID: 5006208
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  • 10. [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; 64(4):194-7. PubMed ID: 4010406
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  • 12. [Waardenburg's syndrome. Clinical and genetical study of a family with affected twins].
    Carakushansky G, Berthier C.
    AMB Rev Assoc Med Bras; 1975 May; 21(5):159-60. PubMed ID: 1088764
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  • 13. Waardenburg syndrome--penetrance of major signs.
    Preus M, Linstrom C, Polomeno RC, Milot J.
    Am J Med Genet; 1983 Jul; 15(3):383-8. PubMed ID: 6881207
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  • 15. Mental retardation and EEG abnormalities in Waardenburg's syndrome: two case reports (EEG anomalies in Waardenburg's syndrome).
    Cantani A, Bamonte G, Tacconi ML.
    Padiatr Padol; 1989 Jul; 24(2):137-40. PubMed ID: 2503803
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  • 17. [Waardenburg's syndrome. Report of a family (author's transl)].
    Gracia R, Burgueros M, Lledó G, Barrio R, Alvarado F.
    An Esp Pediatr; 1975 Jul; 8(4):429-34. PubMed ID: 1147417
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  • 18. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A, Gollop TR, Otto PG.
    Am J Med Genet; 1983 Apr; 14(4):607-15. PubMed ID: 6846395
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  • 19. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome.
    Stoll C, Terzic J, Fischbach M.
    Genet Couns; 1999 Apr; 10(4):337-43. PubMed ID: 10631920
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