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3. Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects. Posch MG; Perrot A; Schmitt K; Mittelhaus S; Esenwein EM; Stiller B; Geier C; Dietz R; Gessner R; Ozcelik C; Berger F Am J Med Genet A; 2008 Jan; 146A(2):251-3. PubMed ID: 18076106 [No Abstract] [Full Text] [Related]
4. Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects. Salazar M; Consoli F; Villegas V; Caicedo V; Maddaloni V; Daniele P; Caianiello G; Pachón S; Nuñez F; Limongelli G; Pacileo G; Marino B; Bernal JE; De Luca A; Dallapiccola B Eur J Med Genet; 2011; 54(3):306-9. PubMed ID: 21276881 [TBL] [Abstract][Full Text] [Related]
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6. Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect. Hirayama-Yamada K; Kamisago M; Akimoto K; Aotsuka H; Nakamura Y; Tomita H; Furutani M; Imamura S; Takao A; Nakazawa M; Matsuoka R Am J Med Genet A; 2005 May; 135(1):47-52. PubMed ID: 15810002 [TBL] [Abstract][Full Text] [Related]
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8. Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects. Alcántara-Ortigoza MA; De Rubens-Figueroa J; Reyna-Fabian ME; Estandía-Ortega B; González-del Angel A; Molina-Álvarez B; Velázquez-Aragón JA; Villagómez-Martínez S; Pereira-López GI; Martínez-Cruz V; Álvarez-Gómez RM; Díaz-García L Pediatr Cardiol; 2015 Apr; 36(4):802-8. PubMed ID: 25524324 [TBL] [Abstract][Full Text] [Related]
9. 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; 17(1):107-9. PubMed ID: 17184575 [TBL] [Abstract][Full Text] [Related]
10. Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects. Hamanoue H; Rahayuningsih SE; Hirahara Y; Itoh J; Yokoyama U; Mizuguchi T; Saitsu H; Miyake N; Hirahara F; Matsumoto N Cardiol Young; 2009 Sep; 19(5):482-5. PubMed ID: 19678963 [TBL] [Abstract][Full Text] [Related]
11. A novel mutation of GATA4 in a familial atrial septal defect. Chen Y; Mao J; Sun Y; Zhang Q; Cheng HB; Yan WH; Choy KW; Li H Clin Chim Acta; 2010 Nov; 411(21-22):1741-5. PubMed ID: 20659440 [TBL] [Abstract][Full Text] [Related]
12. The Aspect of NK2 Transcription Factor Related Locus-5 (NKX2.5) Gene Mutations in Bangladeshi Atrial Septal Defect (ASD) patients and 2D Relationship with their Age. Roy RR; Sultana GN; Begum R; Shahinuzzaman AD; Sharif MI Mymensingh Med J; 2016 Jan; 25(1):79-84. PubMed ID: 26931254 [TBL] [Abstract][Full Text] [Related]
13. Novel NKX2-5 mutations in patients with familial atrial septal defects. Liu XY; Wang J; Yang YQ; Zhang YY; Chen XZ; Zhang W; Wang XZ; Zheng JH; Chen YH Pediatr Cardiol; 2011 Feb; 32(2):193-201. PubMed ID: 21188375 [TBL] [Abstract][Full Text] [Related]
14. GATA4 mutations in 357 unrelated patients with congenital heart malformation. Butler TL; Esposito G; Blue GM; Cole AD; Costa MW; Waddell LB; Walizada G; Sholler GF; Kirk EP; Feneley M; Harvey RP; Winlaw DS Genet Test Mol Biomarkers; 2010 Dec; 14(6):797-802. PubMed ID: 20874241 [TBL] [Abstract][Full Text] [Related]
15. A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype? Gutierrez-Roelens I; De Roy L; Ovaert C; Sluysmans T; Devriendt K; Brunner HG; Vikkula M Eur J Hum Genet; 2006 Dec; 14(12):1313-6. PubMed ID: 16896344 [TBL] [Abstract][Full Text] [Related]
16. 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; 19(1):40-4. PubMed ID: 19049681 [TBL] [Abstract][Full Text] [Related]
17. Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease. Stallmeyer B; Fenge H; Nowak-Göttl U; Schulze-Bahr E Clin Genet; 2010 Dec; 78(6):533-40. PubMed ID: 20456451 [TBL] [Abstract][Full Text] [Related]
18. Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD. Watanabe Y; Benson DW; Yano S; Akagi T; Yoshino M; Murray JC J Med Genet; 2002 Nov; 39(11):807-11. PubMed ID: 12414819 [No Abstract] [Full Text] [Related]
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20. [Mutation of NKX2-5 gene in patients with atrial septal defect]. Liu XY; Yang YQ; Yang Y; Lin XP; Chen YH Zhonghua Er Ke Za Zhi; 2009 Sep; 47(9):696-700. PubMed ID: 20021795 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]