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Journal Abstract Search

148 related items for PubMed ID: 9074723

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  • 4. 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. Diagnosis and penetrance of dystopia canthorum in Waardenburg syndrome type I (WS1).
    Arias S.
    Am J Med Genet; 1984 Apr; 17(4):863-7. PubMed ID: 6720753
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  • 9. Waardenburg syndrome.
    Konno P, Silm H.
    J Eur Acad Dermatol Venereol; 2001 Jul; 15(4):330-3. PubMed ID: 11730045
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  • 10. [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 Jul; 20(5):387-90. PubMed ID: 9238477
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  • 13. [Gene responsible for Waardenburg syndrome type I].
    Tsukamoto K, Niikawa N.
    Tanpakushitsu Kakusan Koso; 1993 Feb; 38(3):361-5. PubMed ID: 8098159
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  • 14. A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.
    Hughes AE, Newton VE, Liu XZ, Read AP.
    Nat Genet; 1994 Aug; 7(4):509-12. PubMed ID: 7951321
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  • 15. 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; 26(2):103-31. PubMed ID: 670940
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  • 16. 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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  • 17. Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1.
    Steel KP, Smith RJ.
    Nat Genet; 1992 Sep; 2(1):75-9. PubMed ID: 1303254
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  • 18. Analysis of variability of clinical manifestations in Waardenburg syndrome.
    Reynolds JE, Meyer JM, Landa B, Stevens CA, Arnos KS, Israel J, Marazita ML, Bodurtha J, Nance WE, Diehl SR.
    Am J Med Genet; 1995 Jul 17; 57(4):540-7. PubMed ID: 7573125
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  • 19. Genetic heterogeneity in the Waardenburg syndrome.
    Arias S.
    Birth Defects Orig Artic Ser; 1971 Mar 17; 07(4):87-101. PubMed ID: 5006208
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