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Journal Abstract Search

154 related items for PubMed ID: 2555708

  • 1. Oto-palato-digital syndrome in an Iranian infant.
    Farhud DD, Walizadeh GR, Farhud I.
    Monatsschr Kinderheilkd; 1989 Oct; 137(10):681-3. PubMed ID: 2555708
    [Abstract] [Full Text] [Related]

  • 2. Oto-palato-digital syndrome with features of type I and II in brothers.
    Horn D, Nitz I, Bollmann R.
    Genet Couns; 1995 Oct; 6(3):233-40. PubMed ID: 8588852
    [Abstract] [Full Text] [Related]

  • 3. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P, Lefort G, Eglin MC, Rieu D, Sarda P.
    Genet Couns; 1993 Oct; 4(4):289-94. PubMed ID: 8110417
    [Abstract] [Full Text] [Related]

  • 4. Oto-palato-digital syndrome type II.
    Stoll C, Alembik Y.
    Genet Couns; 1994 Oct; 5(1):61-6. PubMed ID: 8031537
    [Abstract] [Full Text] [Related]

  • 5. Oto-palato-digital syndrome, type II--an X-linked skeletal dysplasia.
    Brewster TG, Lachman RS, Kushner DC, Holmes LB, Isler RJ, Rimoin DL.
    Am J Med Genet; 1985 Feb; 20(2):249-54. PubMed ID: 3976718
    [Abstract] [Full Text] [Related]

  • 6. On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene.
    Alembik Y, Stoll C, Messer J.
    Genet Couns; 1997 Feb; 8(2):133-7. PubMed ID: 9219012
    [Abstract] [Full Text] [Related]

  • 7.
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  • 8. Oto-palato-digital syndrome type II in two unrelated boys.
    Preis S, Kemperdick H, Majewski F.
    Clin Genet; 1994 Mar; 45(3):154-61. PubMed ID: 8026107
    [Abstract] [Full Text] [Related]

  • 9. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML, Pai GS, Wilkes B, Lebel RR.
    Am J Med Genet; 2001 Aug 15; 102(3):237-42. PubMed ID: 11484200
    [Abstract] [Full Text] [Related]

  • 10. Type III syndactyly and oculodentodigital dysplasia: a clinical spectrum.
    Schrander-Stumpel CT, De Groot-Wijnands JB, De Die-Smulders C, Fryns JP.
    Genet Couns; 1993 Aug 15; 4(4):271-6. PubMed ID: 8110413
    [Abstract] [Full Text] [Related]

  • 11. FG syndrome in a premature male.
    Bianchi DW.
    Am J Med Genet; 1984 Oct 15; 19(2):383-6. PubMed ID: 6507484
    [Abstract] [Full Text] [Related]

  • 12. [A typical case of Smith-Lemli-Opitz syndrome: nosologic problems and overlapping syndromes].
    Camera G.
    Pathologica; 1990 Oct 15; 82(1081):539-42. PubMed ID: 1964208
    [Abstract] [Full Text] [Related]

  • 13. Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.
    Toriello HV, Higgins JV.
    Am J Med Genet; 1995 Jan 16; 55(2):200-4. PubMed ID: 7717418
    [Abstract] [Full Text] [Related]

  • 14. New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies.
    Seaver LH, Cassidy SB.
    Am J Med Genet; 1991 Dec 15; 41(4):405-9. PubMed ID: 1776627
    [Abstract] [Full Text] [Related]

  • 15. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug 15; 12(4):377-409. PubMed ID: 7124793
    [Abstract] [Full Text] [Related]

  • 16. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A, Young-Wee T, Frye T.
    Am J Med Genet; 1983 May 15; 15(1):71-7. PubMed ID: 6859126
    [Abstract] [Full Text] [Related]

  • 17. [Knee pterygium syndrome in a newborn infant].
    Meinecke P, Menzel J, Froster-Iskenius U.
    Monatsschr Kinderheilkd; 1989 Apr 15; 137(4):228-30. PubMed ID: 2543917
    [Abstract] [Full Text] [Related]

  • 18. Polymicrogyria, cerebellar vermis hypoplasia, severe facial dysmorphism and cleft palate: a new syndrome?
    Mosca AL, Laurent N, Guibaud L, Callier P, Thauvin-Robinet C, Mugneret F, Huet F, Grimaldi M, Gouyon JB, Sandre D, Faivre L.
    Eur J Med Genet; 2007 Apr 15; 50(1):48-53. PubMed ID: 17067864
    [Abstract] [Full Text] [Related]

  • 19. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
    Sivasli O, Ozer EA, Ozer A, Aydinlioglu H, Helvaci M.
    Genet Couns; 2007 Apr 15; 18(2):247-50. PubMed ID: 17710878
    [Abstract] [Full Text] [Related]

  • 20. [Syndactylia associated with multiple malformation syndromes. Observation of a new symptomatologic complex in 3 brothers].
    Garau A, Nurchi AM, Melis P, Frau G, Costa G.
    Pediatr Med Chir; 1988 Apr 15; 10(2):227-32. PubMed ID: 2845373
    [Abstract] [Full Text] [Related]

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