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 *

160 related articles for article (PubMed ID: 26036351)

  • 1. Identification of Copy Number Variations in Isolated Tetralogy of Fallot.
    Aguayo-Gómez A; Arteaga-Vázquez J; Svyryd Y; Calderón-Colmenero J; Zamora-González C; Vargas-Alarcón G; Mutchinick OM
    Pediatr Cardiol; 2015 Dec; 36(8):1642-6. PubMed ID: 26036351
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease.
    Li Z; Huang J; Liang B; Zeng D; Luo S; Yan T; Liao F; Huang J; Li J; Cai R; Deng X; Tang N
    J Clin Lab Anal; 2019 Feb; 33(2):e22660. PubMed ID: 30221396
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of gene copy number variations in patients with congenital heart disease using multiplex ligation-dependent probe amplification.
    Mutlu ET; Aykan HH; Karagöz T
    Anatol J Cardiol; 2018 Jul; 20(1):9-15. PubMed ID: 29952356
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
    Zhang X; Xu Y; Liu D; Geng J; Chen S; Jiang Z; Fu Q; Sun K
    BMC Genomics; 2015 May; 16(1):364. PubMed ID: 25952753
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Pilot Study of Multiplex Ligation-Dependent Probe Amplification Evaluation of Copy Number Variations in Romanian Children with Congenital Heart Defects.
    Bolunduț AC; Nazarie F; Lazea C; Șufană C; Miclea D; Lazăr C; Mihu CM
    Genes (Basel); 2024 Feb; 15(2):. PubMed ID: 38397197
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases.
    Nagy O; Szakszon K; Biró BO; Mogyorósy G; Nagy D; Nagy B; Balogh I; Ujfalusi A
    J Biotechnol; 2019 Jun; 299():86-95. PubMed ID: 31054299
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Systemic Screening for 22q11.2 Copy Number Variations in Hungarian Pediatric and Adult Patients With Congenital Heart Diseases Identified Rare Pathogenic Patterns in the Region.
    Zodanu GKE; Oszlánczi M; Havasi K; Kalapos A; Rácz G; Katona M; Ujfalusi A; Nagy O; Széll M; Nagy D
    Front Genet; 2021; 12():635480. PubMed ID: 33995479
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication.
    Pires R; Pires LM; Vaz SO; Maciel P; Anjos R; Moniz R; Branco CC; Cabral R; Carreira IM; Mota-Vieira L
    BMC Genet; 2014 Nov; 15():115. PubMed ID: 25376777
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy.
    Cabuk F; Karabulut HG; Tuncali T; Karademir S; Bozdayi M; Tükün A
    Turk J Pediatr; 2007; 49(1):61-8. PubMed ID: 17479646
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart disease.
    Guida V; Lepri F; Vijzelaar R; De Zorzi A; Versacci P; Digilio MC; Marino B; De Luca A; Dallapiccola B
    Dis Markers; 2010; 28(5):287-92. PubMed ID: 20592452
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.
    Rauch R; Hofbeck M; Zweier C; Koch A; Zink S; Trautmann U; Hoyer J; Kaulitz R; Singer H; Rauch A
    J Med Genet; 2010 May; 47(5):321-31. PubMed ID: 19948535
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Application of array-comparative genomic hybridization in tetralogy of Fallot.
    Liu L; Wang HD; Cui CY; Wu D; Li T; Fan TB; Peng BT; Zhang LZ; Wang CZ
    Medicine (Baltimore); 2016 Dec; 95(49):e5552. PubMed ID: 27930557
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants.
    Griffin HR; Töpf A; Glen E; Zweier C; Stuart AG; Parsons J; Peart I; Deanfield J; O'Sullivan J; Rauch A; Scambler P; Burn J; Cordell HJ; Keavney B; Goodship JA
    Heart; 2010 Oct; 96(20):1651-5. PubMed ID: 20937753
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16.
    Floriani MA; Glaeser AB; Dorfman LE; Agnes G; Rosa RFM; Zen PRG
    J Pediatr Genet; 2021 Jun; 10(2):92-97. PubMed ID: 33996178
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle.
    Dorn C; Perrot A; Grunert M; Rickert-Sperling S
    Adv Exp Med Biol; 2024; 1441():629-644. PubMed ID: 38884738
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ultra high-resolution gene centric genomic structural analysis of a non-syndromic congenital heart defect, Tetralogy of Fallot.
    Bittel DC; Zhou XG; Kibiryeva N; Fiedler S; O'Brien JE; Marshall J; Yu S; Liu HY
    PLoS One; 2014; 9(1):e87472. PubMed ID: 24498113
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications.
    He GW; Maslen CL; Chen HX; Hou HT; Bai XY; Wang XL; Liu XC; Lu WL; Chen XX; Chen WD; Xing QS; Wu Q; Wang J; Yang Q
    Clin Genet; 2022 Nov; 102(5):391-403. PubMed ID: 35882632
    [TBL] [Abstract][Full Text] [Related]  

  • 20. De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
    Greenway SC; Pereira AC; Lin JC; DePalma SR; Israel SJ; Mesquita SM; Ergul E; Conta JH; Korn JM; McCarroll SA; Gorham JM; Gabriel S; Altshuler DM; Quintanilla-Dieck Mde L; Artunduaga MA; Eavey RD; Plenge RM; Shadick NA; Weinblatt ME; De Jager PL; Hafler DA; Breitbart RE; Seidman JG; Seidman CE
    Nat Genet; 2009 Aug; 41(8):931-5. PubMed ID: 19597493
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.