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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

195 related items for PubMed ID: 7268028

  • 41. 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; 6(4):401-4. PubMed ID: 8054982
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  • 45. Pedigree analysis and descriptive investigation of three classic phenotypes associated with Holt-Oram syndrome.
    Lehner R, Goharkhay N, Tringler B, Fasching C, Hengstschläger M.
    J Reprod Med; 2003 Mar; 48(3):153-9. PubMed ID: 12698771
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  • 47. [Genetical basis of Holt-Oram syndrome].
    Rokicka A, Rokicki W.
    Wiad Lek; 1999 Mar; 52(11-12):606-9. PubMed ID: 10745699
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  • 48. [Use and limitations of M-mode echocardiography in the diagnosis of congenital heart disease in the critically-ill newborn (author's transl)].
    Schmaltz AA, Heil RP, Steil E, Teufel M.
    Herz; 1980 Aug; 5(4):213-22. PubMed ID: 7274973
    [No Abstract] [Full Text] [Related]

  • 49. [Holt-Oram syndrome].
    Okuni M.
    Nihon Rinsho; 1977 Aug; 35 Suppl 1():720-1. PubMed ID: 612965
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  • 50. [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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  • 51. A very rare case of polysplenia syndrome with congenital diffuse pulmonary arteriovenous fistulas.
    Gürses D, Ulger Z, Levent E, Ozyürek AR.
    Turk J Pediatr; 2006 Jun 15; 48(1):96-9. PubMed ID: 16562797
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  • 52. 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 Jun 15; 40(4):613-8. PubMed ID: 10028874
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  • 53. Holt-Oram syndrome: an observation in a father and a son.
    Mekanandha V, Subhannachart W, Hathirat S.
    J Med Assoc Thai; 1979 May 15; 62(5):272-6. PubMed ID: 438692
    [No Abstract] [Full Text] [Related]

  • 54. Unexplained right atrial enlargement may be a sign of Holt-Oram syndrome in the fetus.
    Paladini D, Tiesi M, Buffi D, Tuo G, Marasini M.
    Ultrasound Obstet Gynecol; 2014 Apr 15; 43(4):475-6. PubMed ID: 24185902
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  • 55. Unguarded tricuspid valvar orifice in the fetus.
    Wong KK, Farquharson DI, Duncan WJ.
    Cardiol Young; 2004 Oct 15; 14(5):557-9. PubMed ID: 15680079
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  • 56. [Smith-Lemli-Opitz syndrome. Cardiologic considerations (author's transl)].
    Gómez de Terreros I, Cintado Bueno C, Ariza Almeida S, González Meneses A.
    An Esp Pediatr; 1975 Oct 15; 8(6):689-94. PubMed ID: 1211697
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  • 57. [Holt-Oram syndrome (surgical correction by closing the intra-auricular defect and implanting a pacemaker)].
    Senador-Gómez G, Morillo F, Fiz L, Bosch R, Sagrista J, Rivas LE, Grañena J, Abad C, Paravisini J.
    Rev Esp Cardiol; 1978 Oct 15; 31(4):449-52. PubMed ID: 694176
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  • 58. [The Holt-Oram syndrome].
    Walter H, Frank A, Kambhu C.
    Z Kardiol; 1974 Jan 15; 63(1):1-16. PubMed ID: 4411232
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  • 59. [Cerebral venous sinuses thrombosis in an infant with supramitral obstructive membrane associated with partial anomalous pulmonary venous return].
    Smilari P, Romeo MG, Sciacca P, Scalzo G, Gallo C, Mattia C, Manfrè L, Distefano G.
    Minerva Pediatr; 2005 Apr 15; 57(2):111-6. PubMed ID: 15986003
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  • 60. [Staged operation for right isomerism with total anomalous pulmonary venous return: report of a case].
    Yoshida S, Yamagishi M, Syuntou K, Okano T, Yamada Y, Fujiwara K, Kitamura N.
    Kyobu Geka; 2001 Aug 15; 54(9):794-6. PubMed ID: 11517554
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