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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

244 related items for PubMed ID: 9381776

  • 21. Radial club hand and Holt-Oram syndrome.
    Elbaum R, Royer M, Godart S.
    Acta Chir Belg; 1995; 95(5):229-36. PubMed ID: 7502621
    [Abstract] [Full Text] [Related]

  • 22. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome).
    Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, Seidman JG, Seidman CE.
    N Engl J Med; 1994 Mar 31; 330(13):885-91. PubMed ID: 8114858
    [Abstract] [Full Text] [Related]

  • 23. Phocomelia, flexion deformities and absent thumbs: a new hereditary upper limb malformation.
    Holmes LB, Borden S.
    Pediatrics; 1974 Oct 31; 54(4):461-5. PubMed ID: 4415048
    [No Abstract] [Full Text] [Related]

  • 24. Pedigree analysis and descriptive investigation of three classic phenotypes associated with Holt-Oram syndrome.
    Lehner R, Goharkhay N, Tringler B, Fasching C, Hengstschläger M.
    J Reprod Med; 2003 Mar 31; 48(3):153-9. PubMed ID: 12698771
    [Abstract] [Full Text] [Related]

  • 25. TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts.
    Reamon-Buettner SM, Borlak J.
    Hum Mutat; 2004 Jul 31; 24(1):104. PubMed ID: 15221798
    [Abstract] [Full Text] [Related]

  • 26. A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12.
    Bonnet D, Pelet A, Legeai-Mallet L, Sidi D, Mathieu M, Parent P, Plauchu H, Serville F, Schinzel A, Weissenbach J.
    Nat Genet; 1994 Apr 31; 6(4):405-8. PubMed ID: 8054983
    [Abstract] [Full Text] [Related]

  • 27. Holt-Oram syndrome revisited. Two patients in the same family.
    Frota Filho JD, Pereira W, Leiria TL, Vallenas M, Leães PE, Blacher C, Lúcio E, Lucchese FA.
    Arq Bras Cardiol; 1999 Nov 31; 73(5):429-34. PubMed ID: 10887363
    [Abstract] [Full Text] [Related]

  • 28. Prolapsed mitral valve associated with the Holt-Oram syndrome.
    Miller AB, Salcedo EE, Bahler RC.
    Chest; 1975 Feb 31; 67(2):230-2. PubMed ID: 1116403
    [Abstract] [Full Text] [Related]

  • 29. Heart-hand syndrome II. A report of Tabatznik syndrome with new findings.
    Silengo MC, Biagioli M, Guala A, Lopez-Bell G, Lala R.
    Clin Genet; 1990 Aug 31; 38(2):105-13. PubMed ID: 1976459
    [Abstract] [Full Text] [Related]

  • 30. Defining Features of the Upper Extremity in Holt-Oram Syndrome.
    Wall LB, Piper SL, Habenicht R, Oishi SN, Ezaki M, Goldfarb CA.
    J Hand Surg Am; 2015 Sep 31; 40(9):1764-8. PubMed ID: 26243320
    [Abstract] [Full Text] [Related]

  • 31. Muscular involvement in the Holt-Oram syndrome.
    Spranger S, Ulmer H, Tröger J, Jansen O, Graf J, Meinck HM, Spranger M.
    J Med Genet; 1997 Dec 31; 34(12):978-81. PubMed ID: 9429137
    [Abstract] [Full Text] [Related]

  • 32. Upper-limb-cardiovascular syndrome. Two cases of Holt-Oram syndrome.
    Yanase Y, Ueba Y.
    Hand; 1978 Feb 31; 10(1):56-60. PubMed ID: 710983
    [Abstract] [Full Text] [Related]

  • 33. [Holt-Oram syndrome--the importance of early diagnosis and interdisciplinary approach. A case report].
    Zakanj Z.
    Lijec Vjesn; 2013 Feb 31; 135(1-2):12-4. PubMed ID: 23607171
    [Abstract] [Full Text] [Related]

  • 34. Holt-Oram syndrome associated with ectromelia and chromosomal aberrations.
    Rybak M, Kozlowski K, Kleczkowska A, Lewandowska J, Sokolowski J, Soltysik-Wilk E.
    Am J Dis Child; 1971 Jun 31; 121(6):490-5. PubMed ID: 5581016
    [No Abstract] [Full Text] [Related]

  • 35. [Microsurgical tissue transplantation for correction of hand abnormalities].
    Reichert B, Berger A.
    Handchir Mikrochir Plast Chir; 1994 Jul 31; 26(4):200-5;discussion 206. PubMed ID: 7926990
    [Abstract] [Full Text] [Related]

  • 36. [Holt-Oram syndrome with chromosomopathy (author's transl)].
    González Espinosa C, Artiles Pérez L, García Báez M, Otero Gómez A, García Miranda JL.
    An Esp Pediatr; 1982 Jan 31; 16(1):77-81. PubMed ID: 7081854
    [Abstract] [Full Text] [Related]

  • 37.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, McDermott DA, Fong JC, Basson CT.
    ; 1993 Jan 31. PubMed ID: 20301290
    [Abstract] [Full Text] [Related]

  • 38. Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q.
    Terrett JA, Newbury-Ecob R, Cross GS, Fenton I, Raeburn JA, Young ID, Brook JD.
    Nat Genet; 1994 Apr 31; 6(4):401-4. PubMed ID: 8054982
    [Abstract] [Full Text] [Related]

  • 39. The antenatal ultrasonographic detection of the Holt-Oram syndrome.
    Muller LM, De Jong G, Van Heerden KM.
    S Afr Med J; 1985 Aug 31; 68(5):313-5. PubMed ID: 3898414
    [Abstract] [Full Text] [Related]

  • 40. [The syndrome of congenital heart defect with upper extremity abnormalities (Holt-Oram)].
    Rössler J, Frank M, Zizka J.
    Z Kreislaufforsch; 1967 May 31; 56(5):455-63. PubMed ID: 5586386
    [No Abstract] [Full Text] [Related]

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