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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

199 related items for PubMed ID: 2070544

  • 1. 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; 39(4):241-4. PubMed ID: 2070544
    [Abstract] [Full Text] [Related]

  • 2. [The Holt-Oram syndrome. Review of the literature and current orthopedic treatment concepts].
    Weber M, Wenz W, van Riel A, Kaufmann A, Graf J.
    Z Orthop Ihre Grenzgeb; 1997 Apr; 135(4):368-75. PubMed ID: 9381776
    [Abstract] [Full Text] [Related]

  • 3. 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; 73(5):429-34. PubMed ID: 10887363
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. [Diagnosis of familial Holt-Oram syndrome].
    Lehner R, Wenzl R, Vanura H, Frank W, Safar P, Husslein P.
    Z Geburtshilfe Perinatol; 1994 Aug; 198(4):143-9. PubMed ID: 7975801
    [Abstract] [Full Text] [Related]

  • 6. [The Holt-Oram syndrome. Entelechy or clinical entity? A mild form of familial presentation].
    Palma Nieto JC, Herráez García J, Sciaccaluga Morelli C, Briones García JL.
    Rev Esp Cardiol; 1993 Jun; 46(6):385-8. PubMed ID: 8316706
    [Abstract] [Full Text] [Related]

  • 7. An operated case of Holt-Oram syndrome with autosomal dominant inheritance.
    Czakó Z, Gömöry A, Homolay P, Bacsa S, Kiss S, Móricz F, Fülöp F, Papp Z.
    Basic Res Cardiol; 1976 Jun; 71(1):60-7. PubMed ID: 1259686
    [Abstract] [Full Text] [Related]

  • 8. 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; 25(6):1093-8. PubMed ID: 25216260
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. [Characteristics of Holt-Oram syndrome].
    Rozenberg VD.
    Ter Arkh; 1987 Mar 31; 59(4):135-6. PubMed ID: 3589990
    [No Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L, Corsello G, Giuffrè M, Piccione M, Albanese A.
    Am J Med Genet; 1994 Jul 01; 51(3):266-9. PubMed ID: 8074157
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 6(4):405-8. PubMed ID: 8054983
    [Abstract] [Full Text] [Related]

  • 14. Update: PGD and Holt-Oram syndrome.
    McDermott DA, He J, Song YS, Kligman I, Basson CT.
    Am J Med Genet A; 2005 Jul 15; 136(2):223. PubMed ID: 15940699
    [No Abstract] [Full Text] [Related]

  • 15. 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 15; 6(4):401-4. PubMed ID: 8054982
    [Abstract] [Full Text] [Related]

  • 16. Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defects.
    Turnpenny PD, Dean JC, Duffty P, Reid JA, Carter P.
    J Med Genet; 1992 Sep 15; 29(9):659-62. PubMed ID: 1404297
    [Abstract] [Full Text] [Related]

  • 17. [The Holt-Oram syndrome].
    Walter H, Frank A, Kambhu C.
    Z Kardiol; 1974 Jan 15; 63(1):1-16. PubMed ID: 4411232
    [No Abstract] [Full Text] [Related]

  • 18. Clinical expression of Holt-Oram syndrome on the basis of own clinical experience considering prenatal diagnosis.
    Walencka Z, Jamsheer A, Surmiak P, Baumert M, Jezela-Stanek A, Witek A, Materna-Kiryluk A, Latos-Bieleńska A, Socha M, Sowińska-Seidler A.
    Ginekol Pol; 2016 Jan 15; 87(10):706-710. PubMed ID: 27958623
    [Abstract] [Full Text] [Related]

  • 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 15; 16(1):77-81. PubMed ID: 7081854
    [Abstract] [Full Text] [Related]

  • 20. Autosomal dominant inheritance of Weaver syndrome.
    Fryer A, Smith C, Rosenbloom L, Cole T.
    J Med Genet; 1997 May 15; 34(5):418-9. PubMed ID: 9152841
    [Abstract] [Full Text] [Related]

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