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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

305 related items for PubMed ID: 7646274

  • 1. [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; 88(5):661-6. PubMed ID: 7646274
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  • 2. 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; 6(4):405-8. PubMed ID: 8054983
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  • 3. 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
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  • 7. Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.
    Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE.
    Nat Genet; 1997 Jan 31; 15(1):30-5. PubMed ID: 8988165
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  • 8. Genetic heterogeneity of heart-hand syndromes.
    Basson CT, Solomon SD, Weissman B, MacRae CA, Poznanski AK, Prieto F, Ruiz de la Fuente S, Pease WE, Levin SE, Holmes LB.
    Circulation; 1995 Mar 01; 91(5):1326-9. PubMed ID: 7867169
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  • 12. Novel TBX5 mutations in patients with Holt-Oram syndrome.
    Debeer P, Race V, Gewillig M, Devriendt K, Frijns JP.
    Clin Orthop Relat Res; 2007 Sep 01; 462():20-6. PubMed ID: 17534187
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  • 14. Novel TBX5 duplication in a Japanese family with Holt-Oram syndrome.
    Kimura M, Kikuchi A, Ichinoi N, Kure S.
    Pediatr Cardiol; 2015 Jan 01; 36(1):244-7. PubMed ID: 25274398
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  • 15. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
    Li QY, Newbury-Ecob RA, Terrett JA, Wilson DI, Curtis AR, Yi CH, Gebuhr T, Bullen PJ, Robson SC, Strachan T, Bonnet D, Lyonnet S, Young ID, Raeburn JA, Buckler AJ, Law DJ, Brook JD.
    Nat Genet; 1997 Jan 01; 15(1):21-9. PubMed ID: 8988164
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  • 19. [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 01; 16(1):77-81. PubMed ID: 7081854
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  • 20. Holt-Oram syndrome with associated postaxial and central polydactyly. Further evidence for genetic heterogeneity in the Holt-Oram syndrome.
    Fryns JP, Bonnet D, De Smet L.
    Genet Couns; 1996 Jan 01; 7(4):323-4. PubMed ID: 8985738
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