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Journal Abstract Search

167 related items for PubMed ID: 2385482

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  • 3. X-linked recessive inheritance of an orofaciodigital syndrome with partial expression in females and survival of affected males.
    Edwards M, Mulcahy D, Turner G.
    Clin Genet; 1988 Nov; 34(5):325-32. PubMed ID: 3229001
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  • 4. [The Mohr syndrome (orofaciodigital syndrome type II). 1 familial case].
    Cotton JB, Gardet R, Ladreyt JP, Guibaud P.
    Pediatrie; 1979 Nov; 34(3):257-66. PubMed ID: 492868
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  • 10. Letter: Orofaciodigital syndrome.
    Melnick M, Shields ED.
    Clin Genet; 1976 Jul; 10(1):61. PubMed ID: 949866
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  • 12. [Coffin-Lowry syndrome. Description of 2 cases].
    Barajas LO, Rivera H, Fragoso R, Nazara Z, Cantú JM.
    Bol Med Hosp Infant Mex; 1986 Jun; 43(6):378-81. PubMed ID: 3730116
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  • 19. Orofaciodigital syndrome type I in a girl with unilateral tibial pseudarthrosis.
    Orstavik KH, Tangsrud SE, Nordshus T, Finnanger AM, Hellum C, Gjessing E.
    J Med Genet; 1992 Nov; 29(11):827-30. PubMed ID: 1453437
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  • 20. [Orofaciodigital syndrome--a new variant? Psychiatric, neurologic and neuroradiological findings].
    Degner D, Bleich S, Riegel A, Rüther E.
    Fortschr Neurol Psychiatr; 1999 Dec; 67(12):525-8. PubMed ID: 10683749
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