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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

294 related items for PubMed ID: 8730285

  • 1. Holt-Oram syndrome: a clinical genetic study.
    Newbury-Ecob RA, Leanage R, Raeburn JA, Young ID.
    J Med Genet; 1996 Apr; 33(4):300-7. PubMed ID: 8730285
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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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  • 4. 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
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  • 5. 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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  • 6. 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 01; 6(4):401-4. PubMed ID: 8054982
    [Abstract] [Full Text] [Related]

  • 7. Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestations.
    Jhang WK, Lee BH, Kim GH, Lee JO, Yoo HW.
    Cardiol Young; 2015 Aug 01; 25(6):1093-8. PubMed ID: 25216260
    [Abstract] [Full Text] [Related]

  • 8. Holt-Oram syndrome in four half-siblings with unaffected parents: brief clinical report.
    Braulke I, Herzog S, Thies U, Zoll B.
    Clin Genet; 1991 Apr 01; 39(4):241-4. PubMed ID: 2070544
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  • 9. A family of Holt-Oram syndrome.
    Ito M, Misawa T, Fujino M, Ito S, Fukumoto T.
    Jpn Heart J; 1975 Jul 01; 16(4):480-7. PubMed ID: 1152300
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  • 10. Exclusion of linkage to 14q23-24 in a family with Holt-Oram syndrome.
    Ruiz JC, Legius E, Cuppens H, Moens P, Marynen P, Cassiman JJ.
    Clin Genet; 1994 Sep 01; 46(3):257-9. PubMed ID: 7820941
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  • 11. 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 01; 38(2):105-13. PubMed ID: 1976459
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  • 16. TBX5 intragenic duplication: a family with an atypical Holt-Oram syndrome phenotype.
    Patel C, Silcock L, McMullan D, Brueton L, Cox H.
    Eur J Hum Genet; 2012 Aug 01; 20(8):863-9. PubMed ID: 22333898
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  • 20. The upper limb-cardiovascular syndrome (Holt-Oram syndrome). A survey and a report of four cases.
    Sanz G, Nadal-Ginard B, Mata LA, Buentello L.
    Clin Pediatr (Phila); 1973 Dec 01; 12(12):687-91 passim. PubMed ID: 4761183
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