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Journal Abstract Search

62 related items for PubMed ID: 1605267

  • 1. Familial atrial septal defect with prolonged atrioventricular conduction.
    Bosi G, Sensi A, Calzolari E, Scorrano M.
    Am J Med Genet; 1992 Jun 01; 43(3):641. PubMed ID: 1605267
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  • 3. Familial atrial septal defect in the oval fossa with progressive prolongation of the atrioventricular conduction caused by mutations in the NKX2.5 gene.
    Bjørnstad PG, Leren TP.
    Cardiol Young; 2009 Feb 01; 19(1):40-4. PubMed ID: 19049681
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  • 4. Familial atrial septal defect with prolonged atrioventricular conduction.
    Pease WE, Nordenberg A, Ladda RL.
    Circulation; 1976 May 01; 53(5):759-62. PubMed ID: 1260978
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  • 5. [Secundum atrial septal defect with prolonged atrioventricular conduction: an autosomal dominant hereditary cardiac defect (author's transl)].
    Schaede A, Ramacher J.
    Dtsch Med Wochenschr; 1977 Oct 28; 102(43):1552-4. PubMed ID: 913295
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  • 6. Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.
    Rifai L, Maazouzi W, Sefiani A.
    Cardiol Young; 2007 Feb 28; 17(1):107-9. PubMed ID: 17184575
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  • 7. Familial atrial septal defect with prolonged atrioventricular conduction. A syndrome showing the autosomal dominant pattern of inheritance.
    Bizarro RO, Callahan JA, Feldt RH, Kurland LT, Gordon H, Brandenburg RO.
    Circulation; 1970 Apr 28; 41(4):677-83. PubMed ID: 5437412
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  • 8. Autosomal dominant atrial septal defect of ostium secundum type. Report of three families.
    Li Volti S, Distefano G, Garozzo R, Romeo MG, Sciacca P, Mollica F.
    Ann Genet; 1991 Apr 28; 34(1):14-8. PubMed ID: 1952784
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  • 9. [Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case].
    Stéphan E, Ashoush R, Mégarbané A, Kassab R, Salem N, Loiselet J, Bouvagnet P.
    Arch Mal Coeur Vaiss; 2000 May 28; 93(5):641-7. PubMed ID: 10858865
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  • 13. Familial secundum atrial septal defect with dysrhythmia associated with web neck.
    Kiliç Z, Uçar B, Baş F, Dinleyici EC, Sari E.
    Turk J Pediatr; 2002 May 28; 44(1):69-72. PubMed ID: 11858385
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  • 14. Electrophysiological delineation of the specialized atrioventricular conduction system in patients with congenital heart disease. I. Delineation of the His bundle proximal to the membranous septum.
    Krongrad E, Malm JR, Bowman FO, Hoffman BF, Kaiser GA, Waldo AL.
    J Thorac Cardiovasc Surg; 1974 Jun 28; 67(6):875-82. PubMed ID: 4827951
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  • 15. Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: a new midline disorder.
    Mégarbané A, Stephan E, Kassab R, Ashoush R, Salem N, Bouvagnet P, Loiselet J.
    Am J Med Genet; 1999 Mar 19; 83(3):193-200. PubMed ID: 10096596
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  • 16. [Familial occurrence of interatrial communication and pulmonary stenosis].
    Ferreira C, Korkes H, Laredo J, Murad N, Pfeferman A, de Paola AA, Borrotchin L, Kasinsky N, Buffolo E, Barcellini A.
    Arq Bras Cardiol; 1977 Dec 19; 30(6):429-31. PubMed ID: 613999
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  • 18. Holt-Oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family.
    Moens P, De Smet L, Fabry G, Fryns JP.
    Genet Couns; 1993 Dec 19; 4(4):277-80. PubMed ID: 8110414
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  • 19. [Electrophysiologic assessment before and after surgery for atrial defects: influence of volume overload of the right heart on the conduction system].
    Kano Y, Minamikawa O, Maki S, Yasuda T, Yasuda I, Hirai M, Tauchi N, Kimura T, Miki T, Uozumi K.
    Nihon Kyobu Geka Gakkai Zasshi; 1987 Nov 19; 35(11):1974-9. PubMed ID: 3446712
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  • 20. Familial atrial septal defect with prolonged atrioventricular conduction.
    Günal N, Gül S, Kahramanyol O.
    Acta Paediatr Jpn; 1997 Oct 19; 39(5):634-6. PubMed ID: 9363669
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