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Journal Abstract Search

161 related items for PubMed ID: 3229001

  • 1. 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]

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

  • 3. [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 Nov; 31(3):155-61. PubMed ID: 3265608
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. [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]

  • 6. X-linked dominant inherited diseases with lethality in hemizygous males.
    Wettke-Schäfer R, Kantner G.
    Hum Genet; 1983 Jan; 64(1):1-23. PubMed ID: 6873941
    [Abstract] [Full Text] [Related]

  • 7. Orofaciodigital syndrome with mesomelic limb shortening.
    Burn J, Dezateux C, Hall CM, Baraitser M.
    J Med Genet; 1984 Jun; 21(3):189-92. PubMed ID: 6748015
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. A female infant with features of Mohr and Majewski syndromes: variable expression, a genetic compound, or a distinct entity?
    Baraitser M, Burn J, Fixsen J.
    J Med Genet; 1983 Feb; 20(1):65-7. PubMed ID: 6842538
    [Abstract] [Full Text] [Related]

  • 11. [OFD syndrome in a male. Clinical-genetic analysis of 33 families].
    Segni G, Serra A, Mastrangelo R, Polidori G, Massasso J.
    Acta Genet Med Gemellol (Roma); 1970 Oct; 19(4):546-66. PubMed ID: 5512530
    [No Abstract] [Full Text] [Related]

  • 12. Orofaciodigital syndrome, type I: a phenotypic and genetic analysis.
    Melnick M, Shields ED.
    Oral Surg Oral Med Oral Pathol; 1975 Nov; 40(5):599-610. PubMed ID: 1059061
    [Abstract] [Full Text] [Related]

  • 13. [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]

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

  • 15. Abnormalities of the cerebellum in oro-facio-digital syndrome II (Mohr syndrome).
    Annerén G, Gustavson KH, Jòzwiak S, Kjartansson S, Strömberg B.
    Clin Genet; 1990 Jul; 38(1):69-73. PubMed ID: 2387087
    [Abstract] [Full Text] [Related]

  • 16. X-linked Dyggve-Melchior-Clausen syndrome.
    Yunis E, Fontalvo J, Quintero L.
    Clin Genet; 1980 Oct; 18(4):284-90. PubMed ID: 7192195
    [Abstract] [Full Text] [Related]

  • 17. [Freeman-Sheldon syndrome. Description of 2 cases of probable recessive autosomal inheritance].
    Bonioli E, Bellini C, Ruffa G, Lagorio V, Gemme G.
    Minerva Pediatr; 1987 Feb 28; 39(3-4):123-7. PubMed ID: 3587189
    [No Abstract] [Full Text] [Related]

  • 18. Orofaciodigital syndrome I: a case report.
    Gunbay S, Zeytinoglu B, Ozkinay F, Ozkinay C, Oncag A.
    J Clin Pediatr Dent; 1996 Feb 28; 20(4):329-32. PubMed ID: 9151628
    [Abstract] [Full Text] [Related]

  • 19. [The Mohr syndrome (orofaciodigital syndrome type II). 1 familial case].
    Cotton JB, Gardet R, Ladreyt JP, Guibaud P.
    Pediatrie; 1979 Feb 28; 34(3):257-66. PubMed ID: 492868
    [No Abstract] [Full Text] [Related]

  • 20. The oro-facial-digital syndrome.
    Whelan DT, Feldman W, Dost I.
    Clin Genet; 1975 Sep 28; 8(3):205-12. PubMed ID: 1175324
    [Abstract] [Full Text] [Related]

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