147 related articles for article (PubMed ID: 37969115)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.
Reuter MS; Chaturvedi RR; Jobling RK; Pellecchia G; Hamdan O; Sung WWL; Nalpathamkalam T; Attaluri P; Silversides CK; Wald RM; Marshall CR; Williams SG; Keavney BD; Thiruvahindrapuram B; Scherer SW; Bassett AS
Circ Genom Precis Med; 2021 Aug; 14(4):e003410. PubMed ID: 34328347
[TBL] [Abstract][Full Text] [Related]
7. Expanding the phenotype associated with SMARCC2 variants: a fetus with tetralogy of Fallot.
Sun H; Zhang S; Wang J; Zhou X; Zhang H; Yang H; He Y
BMC Med Genomics; 2022 Mar; 15(1):40. PubMed ID: 35241061
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. Pathophysiological Role of Variants of the Promoter Region of CITED2 Gene in Sporadic Tetralogy of Fallot Patients with Cellular Function Verification.
Chen Z; Chen HX; Hou HT; Yin XY; Yang Q; He GW
Biomolecules; 2022 Nov; 12(11):. PubMed ID: 36358994
[TBL] [Abstract][Full Text] [Related]
13. Genetic Variants of
Yin XY; Chen HX; Chen Z; Yang Q; Han J; He GW
Biomolecules; 2023 Feb; 13(2):. PubMed ID: 36830727
[TBL] [Abstract][Full Text] [Related]
14. [Comparison study of whole exome sequencing and targeted panel sequencing in molecular diagnosis of inherited retinal dystrophies].
Liu XZ; Li YY; Yang LP
Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 52(5):836-844. PubMed ID: 33047716
[TBL] [Abstract][Full Text] [Related]
15. Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing.
Shi X; Zhang L; Bai K; Xie H; Shi T; Zhang R; Fu Q; Chen S; Lu Y; Yu Y; Sun K
Comput Struct Biotechnol J; 2020; 18():381-392. PubMed ID: 32128068
[TBL] [Abstract][Full Text] [Related]
16. Genetic insights into non-syndromic Tetralogy of Fallot.
Althali NJ; Hentges KE
Front Physiol; 2022; 13():1012665. PubMed ID: 36277185
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. A New Family with a Novel
Börklü E; Altunoğlu U; Eraslan S; Kayserili H
Mol Syndromol; 2022 May; 13(3):206-211. PubMed ID: 35707595
[No Abstract] [Full Text] [Related]
[Next] [New Search]