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PUBMED FOR HANDHELDS

Journal Abstract Search


167 related items for PubMed ID: 2385482

  • 1. [A new genetic variant of the orofaciodigital syndrome].
    Bochkova DN, Ternova TI.
    Pediatriia; 1990; (3):95-6. PubMed ID: 2385482
    [No Abstract] [Full Text] [Related]

  • 2. [Case of Arskog is syndrome].
    Chen TP, Romanenko OP, Shats VIa, Sandomirskaia LM, Azarova VIa.
    Pediatriia; 1980 Apr; (4):60-1. PubMed ID: 7189853
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [No Abstract] [Full Text] [Related]

  • 5. Familial orofaciodigital syndrome type I presenting as adult polycystic kidney disease.
    Donnai D, Kerzin-Storrar L, Harris R.
    J Med Genet; 1987 Feb; 24(2):84-7. PubMed ID: 3560172
    [Abstract] [Full Text] [Related]

  • 6. [Description of an orofaciodigital syndrome].
    Joosen E, Legrand W.
    Acta Stomatol Belg; 1982 Feb; 79(1):45-54. PubMed ID: 6954841
    [No Abstract] [Full Text] [Related]

  • 7. [Oto-palato-digital type I syndrome in five generations. Relationship to the type II form].
    Le Marec B, Odent S, Bracq E, Bulard MB, Bourdinière J, Babut JM.
    Ann Genet; 1988 Feb; 31(3):155-61. PubMed ID: 3265608
    [Abstract] [Full Text] [Related]

  • 8. Coffin-Lowry syndrome in an Afro-American family.
    Kousseff BG.
    Am J Med Genet; 1982 Mar; 11(3):373-5. PubMed ID: 7081302
    [No Abstract] [Full Text] [Related]

  • 9. [Orofaciodigital syndrome type I in a mother and daughter].
    Guerrero Vázquez J, Cazenave Bernal A, de Paz Aparicio P, Luengo Casasola JL, Garcés Ramos A, López Vázquez JL, Hoyos Madrid JJ.
    An Esp Pediatr; 1988 Jan; 28(1):59-62. PubMed ID: 3279888
    [Abstract] [Full Text] [Related]

  • 10. Letter: Orofaciodigital syndrome.
    Melnick M, Shields ED.
    Clin Genet; 1976 Jul; 10(1):61. PubMed ID: 949866
    [No Abstract] [Full Text] [Related]

  • 11. Orofaciodigital syndrome type IV: report of a patient.
    Nevin NC, Thomas PS.
    Am J Med Genet; 1989 Feb; 32(2):151-4. PubMed ID: 2929654
    [Abstract] [Full Text] [Related]

  • 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
    [No Abstract] [Full Text] [Related]

  • 13. [Oral-facial-digital syndrome in male (author's transl)].
    Gracia R, Prieto G, Pérez Rodríguez J, Lledó G, Herráiz JI, Jover P.
    An Esp Pediatr; 1976 Jun; 9(1):79-84. PubMed ID: 1267303
    [Abstract] [Full Text] [Related]

  • 14. Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1.
    Cohen MM, Charrow J, Nadler HL.
    Am J Hum Genet; 1981 Jul; 33(4):649-50. PubMed ID: 7258190
    [No Abstract] [Full Text] [Related]

  • 15. [Mohr syndrome--symptoms and differential diagnosis].
    Raschke N, Herrmann FH, Herrmann MC.
    Zahn Mund Kieferheilkd Zentralbl; 1985 Jul; 73(2):155-60. PubMed ID: 3160185
    [No Abstract] [Full Text] [Related]

  • 16. [Brachmann-Cornelia de Lange syndrome].
    Bonioli E, Bellini C, Ruffa G, Camera G, Gemme G.
    Minerva Pediatr; 1987 Feb 28; 39(3-4):135-8. PubMed ID: 3587191
    [No Abstract] [Full Text] [Related]

  • 17. [The diagnosis of Cohen's syndrome].
    Krajewska-Walasek M, Chrzanowska K, Rump Z.
    Wiad Lek; 1986 Sep 15; 39(18):1270-7. PubMed ID: 3564466
    [No Abstract] [Full Text] [Related]

  • 18. [Mohr's syndrome : type II orofaciodigital syndrome (author's transl)].
    Ajacques JC.
    Rev Stomatol Chir Maxillofac; 1981 Sep 15; 82(4):234-40. PubMed ID: 6269173
    [Abstract] [Full Text] [Related]

  • 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 15; 29(11):827-30. PubMed ID: 1453437
    [Abstract] [Full Text] [Related]

  • 20. [Orofaciodigital syndrome--a new variant? Psychiatric, neurologic and neuroradiological findings].
    Degner D, Bleich S, Riegel A, Rüther E.
    Fortschr Neurol Psychiatr; 1999 Dec 15; 67(12):525-8. PubMed ID: 10683749
    [Abstract] [Full Text] [Related]


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