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Journal Abstract Search

173 related items for PubMed ID: 2316963

  • 1. [Waardenburg syndrome. Report of a familial case].
    Khaldi F, Serbegi M, Mokadem H, Lazzem B, Bennaceur B.
    Ann Pediatr (Paris); 1990 Jan; 37(1):55-8. PubMed ID: 2316963
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  • 2. [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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  • 4. 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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  • 5. [Atypical manifestations in familial type 1 Waardenburg syndrome].
    Sans B, Calvas P, Bazex J.
    Ann Dermatol Venereol; 1998 Jan; 125(1):37-41. PubMed ID: 9747206
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  • 6. 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 Jan; 24(2):137-40. PubMed ID: 2503803
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  • 7. Incidences of dystopia canthorum and some other signs in a family with Waardenburg syndrome type I.
    Yoshino M, Nakao M, Shiotsuki Y, Nishiyori A, Yamashita F, Karukaya S, Yoshimura H, Nishida H, Shiotani N, Sugita A.
    Jinrui Idengaku Zasshi; 1986 Dec; 31(4):373-8. PubMed ID: 3613244
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  • 8. 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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  • 9. [Make a diagnosis. Waardenburg's syndrome type 1].
    Aksu F.
    Padiatr Padol; 1983 Jul; 18(4):399-402. PubMed ID: 6646790
    [No Abstract] [Full Text] [Related]

  • 10. Type II Waardenburg syndrome.
    Varughese S, Kumar A, Rao S, Puliyel JM.
    Indian Pediatr; 1988 Apr; 25(4):384-6. PubMed ID: 3225049
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  • 11. [Waardenburg syndrome: neonatal diagnosis apropos of a case].
    Nacher Fernández A, Vitoria Miñana I, Aguilera Olmos R, Buesa Ibáñez E.
    An Esp Pediatr; 1984 Jun; 20(9):911-3. PubMed ID: 6486586
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  • 12. Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).
    Ishikiriyama S, Tonoki H, Shibuya Y, Chin S, Harada N, Abe K, Niikawa N.
    Am J Med Genet; 1989 Aug; 33(4):505-7. PubMed ID: 2596512
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  • 13. Autosomal dominant inheritance of Klein-Waardenburg syndrome.
    Sheffer R, Zlotogora J.
    Am J Med Genet; 1992 Feb 01; 42(3):320-2. PubMed ID: 1536170
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  • 18. [A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC].
    Bassabi SK, Medji AP, Doutetien C, Oussa G, Hounkpe YY, Vodouhe SJ, Babagbeto M, Latoundji S.
    J Fr Ophtalmol; 1997 Feb 01; 20(5):387-90. PubMed ID: 9238477
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