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Journal Abstract Search

240 related items for PubMed ID: 442759

  • 1. [Report of a family with Holt-Oram syndrome (author's transl)].
    Gaul G, Titscher G, Brand O, Heeger H.
    Z Kardiol; 1979 Mar; 68(3):173-5. PubMed ID: 442759
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  • 2. Variable clinical expression of Holt-Oram syndrome in three generations.
    Oğur G, Gül D, Lenk MK, Imirzalioğlu N, Alpay F, Oğur E.
    Turk J Pediatr; 1998 Mar; 40(4):613-8. PubMed ID: 10028874
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  • 9. [An unusual type of congenital heart disease associated with the Holt-Oram-syndrome (author's transl)].
    Ruzić B, Bosnar B, Beleznay O.
    Radiologe; 1981 Jun; 21(6):296-9. PubMed ID: 7268028
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  • 10. Holt-Oram syndrome presenting as agenesis of the left pericardium.
    Dias RR, Albuquerque JM, Pereira AC, Stolf NA, Krieger JE, Mady C, Oliveira SA.
    Int J Cardiol; 2007 Jan 02; 114(1):98-100. PubMed ID: 16376438
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  • 11. [Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome].
    Bonnet D, Terrett J, Pequignot-Viegas E, Weissenbach J, Munnich A, Lyonnet S, Kachaner J.
    Arch Mal Coeur Vaiss; 1995 May 02; 88(5):661-6. PubMed ID: 7646274
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  • 15. [Holt-Oram syndrome (apropos of a familial case concerning 5 generations)].
    Giraud F, Bertozzi JB, Mattei JF, Gerard R, Bernard R.
    Arch Fr Pediatr; 1974 Oct 02; 31(8):765-74. PubMed ID: 4462497
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  • 19. Variation in severity of cardiac disease in Holt-Oram syndrome.
    Sletten LJ, Pierpont ME.
    Am J Med Genet; 1996 Oct 16; 65(2):128-32. PubMed ID: 8911604
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  • 20. 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 16; 6(4):401-4. PubMed ID: 8054982
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