These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
153 related articles for article (PubMed ID: 33942857)
1. Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot. Kalayinia S; Maleki M; Mahdavi M; Mahdieh N Lab Med; 2021 Nov; 52(6):614-618. PubMed ID: 33942857 [TBL] [Abstract][Full Text] [Related]
2. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot. Page DJ; Miossec MJ; Williams SG; Monaghan RM; Fotiou E; Cordell HJ; Sutcliffe L; Topf A; Bourgey M; Bourque G; Eveleigh R; Dunwoodie SL; Winlaw DS; Bhattacharya S; Breckpot J; Devriendt K; Gewillig M; Brook JD; Setchfield KJ; Bu'Lock FA; O'Sullivan J; Stuart G; Bezzina CR; Mulder BJM; Postma AV; Bentham JR; Baron M; Bhaskar SS; Black GC; Newman WG; Hentges KE; Lathrop GM; Santibanez-Koref M; Keavney BD Circ Res; 2019 Feb; 124(4):553-563. PubMed ID: 30582441 [TBL] [Abstract][Full Text] [Related]
3. GATA4 loss-of-function mutations underlie familial tetralogy of fallot. Yang YQ; Gharibeh L; Li RG; Xin YF; Wang J; Liu ZM; Qiu XB; Xu YJ; Xu L; Qu XK; Liu X; Fang WY; Huang RT; Xue S; Nemer G Hum Mutat; 2013 Dec; 34(12):1662-71. PubMed ID: 24000169 [TBL] [Abstract][Full Text] [Related]
4. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595 [TBL] [Abstract][Full Text] [Related]
5. Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot. Wang J; Lu Y; Chen H; Yin M; Yu T; Fu Q Pathology; 2011 Jun; 43(4):322-6. PubMed ID: 21519287 [TBL] [Abstract][Full Text] [Related]
6. GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot. El Bouchikhi I; Belhassan K; Moufid FZ; Houssaini MI; Bouguenouch L; Samri I; Bouhrim M; Ouldim K; Atmani S Afr Health Sci; 2018 Dec; 18(4):922-930. PubMed ID: 30766556 [TBL] [Abstract][Full Text] [Related]
7. Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot. Baban A; Postma AV; Marini M; Trocchio G; Santilli A; Pelegrini M; Sirleto P; Lerone M; Albanese SB; Barnett P; Boogerd CJ; Dallapiccola B; Digilio MC; Ravazzolo R; Pongiglione G Am J Med Genet A; 2014 Dec; 164A(12):3100-7. PubMed ID: 25263169 [TBL] [Abstract][Full Text] [Related]
8. GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease. Kalayinia S; Maleki M; Rokni-Zadeh H; Changi-Ashtiani M; Ahangar H; Biglari A; Shahani T; Mahdieh N J Clin Lab Anal; 2019 Sep; 33(7):e22923. PubMed ID: 31115957 [TBL] [Abstract][Full Text] [Related]
9. Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart. Esposito G; Butler TL; Blue GM; Cole AD; Sholler GF; Kirk EP; Grossfeld P; Perryman BM; Harvey RP; Winlaw DS Am J Med Genet A; 2011 Oct; 155A(10):2416-21. PubMed ID: 22043484 [TBL] [Abstract][Full Text] [Related]
10. New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle. De Luca A; Sarkozy A; Ferese R; Consoli F; Lepri F; Dentici ML; Vergara P; De Zorzi A; Versacci P; Digilio MC; Marino B; Dallapiccola B Clin Genet; 2011 Aug; 80(2):184-90. PubMed ID: 20807224 [TBL] [Abstract][Full Text] [Related]
11. The Functional Polymorphism R129W in the Shi Y; Li Y; Wang Y; Zhuang J; Wang H; Hu M; Mo X; Yue S; Chen Y; Fan X; Chen J; Cai W; Zhu X; Wan Y; Zhong Y; Ye X; Li F; Zhou Z; Dai G; Luo R; Ocorr K; Jiang Z; Li X; Zhu P; Wu X; Yuan W Genet Test Mol Biomarkers; 2019 Sep; 23(9):601-609. PubMed ID: 31386585 [No Abstract] [Full Text] [Related]
12. A novel de novo dominant mutation of NOTCH1 gene in an Iranian family with non-syndromic congenital heart disease. Kalayinia S; Maleki M; Mahdavi M; Mahdieh N J Clin Lab Anal; 2020 Apr; 34(4):e23147. PubMed ID: 31867804 [TBL] [Abstract][Full Text] [Related]
13. Functionally significant, novel GATA4 variants are frequently associated with Tetralogy of Fallot. Dixit R; Narasimhan C; Balekundri VI; Agrawal D; Kumar A; Mohapatra B Hum Mutat; 2018 Dec; 39(12):1957-1972. PubMed ID: 30152191 [TBL] [Abstract][Full Text] [Related]
14. Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot. Alrayes N; Mallah BA; Issa NM; Banaganapalli B; Ahmad Shaik N; Nasser KK; Alshehri BA; Bhuiyan ZA; Bdier AY; Al-Aama JY Gene; 2023 Jan; 851():146909. PubMed ID: 36162527 [TBL] [Abstract][Full Text] [Related]
15. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children. Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692 [TBL] [Abstract][Full Text] [Related]
16. Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia. Ansari H; Mohammadi-Asl J; Hajjari M; Tahmasebi-Birgani M; Kollaee A; Jassemi-Zergani F; Vakili-Hajiagha A J Gene Med; 2019 Aug; 21(8):e3103. PubMed ID: 31177591 [TBL] [Abstract][Full Text] [Related]
17. Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease. Xiong F; Li Q; Zhang C; Chen Y; Li P; Wei X; Li Q; Zhou W; Li L; Shang X; Xu X Cardiovasc Pathol; 2013; 22(2):141-5. PubMed ID: 22959235 [TBL] [Abstract][Full Text] [Related]
18. A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot. Nemer G; Fadlalah F; Usta J; Nemer M; Dbaibo G; Obeid M; Bitar F Hum Mutat; 2006 Mar; 27(3):293-4. PubMed ID: 16470721 [TBL] [Abstract][Full Text] [Related]
19. GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease. Zhang WM; Li XF; Ma ZY; Zhang J; Zhou SH; Li T; Shi L; Li ZZ Chin Med J (Engl); 2009 Feb; 122(4):416-9. PubMed ID: 19302747 [TBL] [Abstract][Full Text] [Related]