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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

175 related items for PubMed ID: 1996196

  • 1.
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  • 2. 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; 15(1):30-5. PubMed ID: 8988165
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  • 3. 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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  • 5. [Mitral prolapse and the Holt-Oram syndrome. Study of a family].
    Masotti G, Ieri A, Castellani S.
    Cardiol Prat; 1978 Jan 02; 29(2):105-10. PubMed ID: 753519
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  • 6. [Deformities of the extremities in Holt-Oram syndrome].
    Hupfauer W, Seling A.
    Z Orthop Ihre Grenzgeb; 1971 May 02; 109(2):270-6. PubMed ID: 4254058
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  • 9. 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 02; 6(4):405-8. PubMed ID: 8054983
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  • 10. [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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  • 13. [Multiple abnormalities (Holt-Oram syndrome)].
    Compagnoni G, Giraldi L, Letterese P.
    Minerva Pediatr; 1978 Dec 31; 30(24):1987-90. PubMed ID: 753964
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  • 16. 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
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  • 18. Holt-Oram syndrome.
    Lichiardopol C, Militaru C, Popescu B, Hila G, Mixich F.
    Rom J Morphol Embryol; 2007 Apr 31; 48(1):67-70. PubMed ID: 17502954
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  • 20. [Case of "upper limb-cardiovascular syndrome" (Holt-Oram syndrome)].
    Polimeno M, Fadda C, Abate M, Morieri M, Del Vecchio E.
    Minerva Pediatr; 1982 Jun 15; 34(11):511-6. PubMed ID: 7132932
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