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.
80 related articles for article (PubMed ID: 21323574)
21. [Association study of the polymorphisms of monoamine oxidase A genes with schizophrenia]. Shi YZ; Wang CH; Lv LX; Wang YH; Zhang HX; Lou BY Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):457-9. PubMed ID: 17680543 [TBL] [Abstract][Full Text] [Related]
23. Polymorphisms of IL23R and Vogt-Koyanagi-Harada syndrome in a Chinese Han population. Jiang Z; Yang P; Hou S; Li F; Zhou H Hum Immunol; 2010 Apr; 71(4):414-7. PubMed ID: 20116410 [TBL] [Abstract][Full Text] [Related]
24. Association of CDH1 promoter polymorphism and the risk of non-syndromic orofacial clefts in a Chinese Han population. Song Y; Zhang S Arch Oral Biol; 2011 Jan; 56(1):68-72. PubMed ID: 20880515 [TBL] [Abstract][Full Text] [Related]
25. Association study and meta-analysis of Alzheimer's disease risk and presenilin-1 intronic polymorphism. Rodríguez-Manotas M; Amorín-Díaz M; Cañizares-Hernández F; Ruíz-Espejo F; Martínez-Vidal S; González-Sarmiento R; Martínez-Hernández P; Cabezas-Herrera J Brain Res; 2007 Sep; 1170():119-28. PubMed ID: 17719017 [TBL] [Abstract][Full Text] [Related]
26. [Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene]. Zhang XN; Ruan LM; Le YP; Zhang Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):322-4. PubMed ID: 12903043 [TBL] [Abstract][Full Text] [Related]
27. MDR1 C3435T polymorphism in patients with breast cancer. Turgut S; Yaren A; Kursunluoglu R; Turgut G Arch Med Res; 2007 Jul; 38(5):539-44. PubMed ID: 17560460 [TBL] [Abstract][Full Text] [Related]
28. Association of DARS gene polymorphisms with the risk of isolated ventricular septal defects in the Chinese Han population. Feng Y; Chen R; Mo X Ital J Pediatr; 2016 Nov; 42(1):102. PubMed ID: 27871331 [TBL] [Abstract][Full Text] [Related]
29. Analysis of RTN4 3'UTR insertion/deletion polymorphisms in ventricular septal defect in a Chinese Han population. Chen Y; Zhou B; Li H; Peng Y; Wang Y; Rao L DNA Cell Biol; 2011 May; 30(5):323-7. PubMed ID: 21166502 [TBL] [Abstract][Full Text] [Related]
30. TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population. Yang L; Gao X; Luo H; Huang Q; Su D; Tan X; Lu C Genet Test Mol Biomarkers; 2017 May; 21(5):312-315. PubMed ID: 28346832 [TBL] [Abstract][Full Text] [Related]
31. Genetic analysis of the TBX3 gene promoter in ventricular septal defects. Chen D; Qiao Y; Meng H; Pang S; Huang W; Zhang H; Yan B Gene; 2013 Jan; 512(2):185-8. PubMed ID: 23116943 [TBL] [Abstract][Full Text] [Related]
32. First report of polymorphisms in MTRR, GATA4, VEGF, and ISL1 genes in Pakistani children with isolated ventricular septal defects (VSD). Sarwar S; Ehsan F; Shabana ; Tahir A; Jamil M; Shahid SU; Khan A; Hasnain S Ital J Pediatr; 2021 Mar; 47(1):70. PubMed ID: 33757570 [TBL] [Abstract][Full Text] [Related]
33. Association of TGFBR2 rs6785358 Polymorphism with Increased Risk of Congenital Ventricular Septal Defect in a Chinese Population. Li XT; Shen CQ; Zhang R; Shi JK; Li ZH; Liu HY; Sun B; Wang K; Yan LR Pediatr Cardiol; 2015 Oct; 36(7):1476-82. PubMed ID: 26022443 [TBL] [Abstract][Full Text] [Related]
34. FLT4 gene polymorphisms influence isolated ventricular septal defect predisposition in a Southwest China population. Zhang Y; Dong X; Zhang J; Zhao M; Wang J; Chu J; Yang Z; Ma S; Lin K; Sun H; Luo Z BMC Med Genomics; 2024 Aug; 17(1):197. PubMed ID: 39107825 [TBL] [Abstract][Full Text] [Related]
35. Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis. Scott AP; Laing NG; Mastaglia F; Dalakas M; Needham M; Allcock RJ J Neuroimmunol; 2012 Sep; 250(1-2):66-70. PubMed ID: 22732452 [TBL] [Abstract][Full Text] [Related]
36. Genetic analysis of the TBX20 gene promoter region in patients with ventricular septal defects. Qiao Y; Wanyan H; Xing Q; Xie W; Pang S; Shan J; Yan B Gene; 2012 May; 500(1):28-31. PubMed ID: 22465533 [TBL] [Abstract][Full Text] [Related]
37. Association between ISL1 variants and susceptibility to ventricular septal defect in a Chinese cohort. Lang J; Tian W; Sun X Mol Diagn Ther; 2013 Apr; 17(2):101-6. PubMed ID: 23572340 [TBL] [Abstract][Full Text] [Related]
38. Novel and functional sequence variants within the TBX2 gene promoter in ventricular septal defects. Pang S; Liu Y; Zhao Z; Huang W; Chen D; Yan B Biochimie; 2013 Sep; 95(9):1807-9. PubMed ID: 23727221 [TBL] [Abstract][Full Text] [Related]
39. Exploring Genetic Diversity of SOD2 and POU5F1 for Congenital Heart Disease in the Southwest Chinese Population. Jin Y; Zhang J; Guo Q; Dong X; Li J; Wang J; Li S; Shen Y; Lin K; Yang Z; Chu J; Sun H; Luo Z Int Heart J; 2024; 65(4):723-729. PubMed ID: 39085111 [TBL] [Abstract][Full Text] [Related]
40. Association between polymorphisms in IL27 and risk for CHD in a Chinese population. Zhang D; Ma M; Yang Y; Wan L; Yang Z; Lv J; Li X; Yang H; Huang P; Li L Cardiol Young; 2016 Feb; 26(2):237-43. PubMed ID: 25662568 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]