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Journal Abstract Search
101 related items for PubMed ID: 5437412
1. 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; 41(4):677-83. PubMed ID: 5437412 [No Abstract] [Full Text] [Related]
2. Familial atrial septal defect with atrioventricular conduction defects. Mandorla S, Martino C. G Ital Cardiol; 1998 Mar; 28(3):294-6. PubMed ID: 9561886 [Abstract] [Full Text] [Related]
4. 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 [No Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. [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 [Abstract] [Full Text] [Related]
8. [Fetal atrioventricular septal defect associated with Patau and Edwards syndromes, as well as trisomy 22]. Cesko I, Hajdú J, Marton T, Tóth-Pál E, Papp C, Papp Z. Orv Hetil; 1998 May 03; 139(18):1087-9. PubMed ID: 9608772 [Abstract] [Full Text] [Related]
9. Familial atrial septal defect with prolonged atrioventricular conduction. Günal N, Gül S, Kahramanyol O. Acta Paediatr Jpn; 1997 Oct 03; 39(5):634-6. PubMed ID: 9363669 [Abstract] [Full Text] [Related]
10. Association of secundum atrial septal defect with abnormalities of atrioventricular conduction or left axis deviation. Genetic study of 10 families. Emanuel R, O'Brien K, Somerville J, Jefferson K, Hegde M. Br Heart J; 1975 Oct 03; 37(10):1085-92. PubMed ID: 1191421 [Abstract] [Full Text] [Related]
11. Familial atrioventricular septal defect: possible genetic mechanisms. Kumar A, Williams CA, Victorica BE. Br Heart J; 1994 Jan 03; 71(1):79-81. PubMed ID: 8297702 [Abstract] [Full Text] [Related]
12. [Familial forms of interauricular communication of the ostium secundum type]. Thomas D, Lascault G, Caille B, Drobinski G, Huberman JP, Shqueir A, Grosgogeat Y. Arch Mal Coeur Vaiss; 1985 Aug 03; 78(8):1205-9. PubMed ID: 3935078 [Abstract] [Full Text] [Related]
13. Secundum type atrial septal defect with prolonged PR interval and autosomal dominant mode of inheritance. Björnstad PG. Br Heart J; 1974 Dec 03; 36(12):1149-54. PubMed ID: 4441445 [No Abstract] [Full Text] [Related]
14. [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 03; 93(5):641-7. PubMed ID: 10858865 [Abstract] [Full Text] [Related]
16. [Autosomal dominant hereditary atrial septal defect with heart conduction defects and mitral valve insufficiency]. Weikl A, Rott HD, Lang E. Z Kardiol; 1976 Jul 03; 65(7):606-15. PubMed ID: 960976 [Abstract] [Full Text] [Related]
17. 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 [Abstract] [Full Text] [Related]
19. Tricuspid atresia and annular hypoplasia: report of a familial occurrence. Kumar A, Victorica BE, Gessner IH, Alexander JA. Pediatr Cardiol; 1994 Mar 19; 15(4):201-3. PubMed ID: 7991439 [Abstract] [Full Text] [Related]
20. Genetics and congenital heart disease. Emanuel R. Br Heart J; 1970 May 19; 32(3):281-91. PubMed ID: 4246190 [Abstract] [Full Text] [Related] Page: [Next] [New Search]