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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 29291004)

  • 1. Whole exome sequencing identifies novel mutation in eight Chinese children with isolated tetralogy of Fallot.
    Liu L; Wang HD; Cui CY; Qin YY; Fan TB; Peng BT; Zhang LZ; Wang CZ
    Oncotarget; 2017 Dec; 8(63):106976-106988. PubMed ID: 29291004
    [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. Whole exome sequencing identifies novel inherited genetic variants in tetralogy of Fallot.
    Pan Y; Liu M; Zhang S; Mei H; Wu J
    J Thorac Dis; 2022 Aug; 14(8):3008-3015. PubMed ID: 36071769
    [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. Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot.
    Pan Y; Liu M; Zhang S; Mei H; Wu J
    Transl Pediatr; 2023 Oct; 12(10):1835-1841. PubMed ID: 37969115
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Case Report: Tetralogy of Fallot in a Chinese Family Caused by a Novel Missense Variant of
    Wang J; Wang C; Xie H; Feng X; Wei L; Wang B; Li T; Pi M; Gong L
    Front Cardiovasc Med; 2022; 9():863650. PubMed ID: 35872890
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Targeted, Next-Generation Genetic Sequencing Study on Tetralogy of Fallot, Combined With Cleft Lip and Palate.
    Liu L; Bu H; Yang Y; Tan Z; Zhang F; Hu S; Zhao T
    J Craniofac Surg; 2017 Jun; 28(4):e351-e355. PubMed ID: 28230599
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Family-based whole-genome sequencing identifies compound heterozygous protein-coding and noncoding mutations in tetralogy of Fallot.
    Wang Y; Jiang T; Tang P; Wu Y; Jiang Z; Dai J; Gu Y; Xu J; Da M; Ma H; Jin G; Mo X; Li Q; Wang X; Hu Z
    Gene; 2020 May; 741():144555. PubMed ID: 32165302
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors.
    Tang CSM; Mononen M; Lam WY; Jin SC; Zhuang X; Garcia-Barcelo MM; Lin Q; Yang Y; Sahara M; Eroglu E; Chien KR; Hong H; Tam PKH; Gruber PJ
    JCI Insight; 2022 Jan; 7(2):. PubMed ID: 34905512
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic Networks.
    Lahm H; Schön P; Doppler S; Dreßen M; Cleuziou J; Deutsch MA; Ewert P; Lange R; Krane M
    Curr Genomics; 2015 Jun; 16(3):141-58. PubMed ID: 26069455
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot.
    Bansal V; Dorn C; Grunert M; Klaassen S; Hetzer R; Berger F; Sperling SR
    PLoS One; 2014; 9(1):e85375. PubMed ID: 24400131
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Peritoneal dialysis in an adult patient with tetralogy of Fallot diagnosed with incomplete Alagille syndrome.
    Ponikowska M; Pollak A; Kotwica-Strzalek E; Brodowska-Kania D; Mosakowska M; Ploski R; Niemczyk S
    BMC Med Genet; 2020 Oct; 21(1):195. PubMed ID: 33008311
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Loss of function in
    Kruszka P; Tanpaiboon P; Neas K; Crosby K; Berger SI; Martinez AF; Addissie YA; Pongprot Y; Sittiwangkul R; Silvilairat S; Makonkawkeyoon K; Yu L; Wynn J; Bennett JT; Mefford HC; Reynolds WT; Liu X; Mommersteeg MTM; Chung WK; Lo CW; Muenke M
    J Med Genet; 2017 Dec; 54(12):825-829. PubMed ID: 28592524
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot.
    Harvey DC; Verma R; Sedaghat B; Hjelm BE; Morton SU; Seidman JG; Kumar SR
    Front Cardiovasc Med; 2023; 10():1249605. PubMed ID: 37840956
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot.
    Chelu A; Williams SG; Keavney BD; Talavera D
    J Hum Genet; 2022 Oct; 67(10):613-615. PubMed ID: 35718831
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Role of fibrillin-1 genetic mutations and polymorphism in aortic dilatation in patients undergoing intracardiac repair of tetralogy of Fallot.
    Chowdhury UK; Mishra AK; Balakrishnan P; Sharma S; Kabra M; Ray R; Kalaivani M; Gupta R; Govindappa RM; Subramaniam GK
    J Thorac Cardiovasc Surg; 2008 Sep; 136(3):757-66, 766.e1-10. PubMed ID: 18805282
    [TBL] [Abstract][Full Text] [Related]  

  • 19. San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease.
    Gelb BD; Towbin JA; McCabe ER; Sujansky E
    Am J Med Genet; 1991 Sep; 40(4):471-6. PubMed ID: 1746613
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The aortic arch in tetralogy of Fallot: types of branching and clinical implications.
    Prabhu S; Kasturi S; Mehra S; Tiwari R; Joshi A; John C; Karl TR
    Cardiol Young; 2020 Aug; 30(8):1144-1150. PubMed ID: 32638692
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.