164 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]