Qiao D - Search Results

1

Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population.

Chen Z, Tang NL, Cao X, Qiao D, Yi L, Cheng JC, Qiu Y. Chen Z, et al. Among authors: qiao d. Eur J Hum Genet. 2009 Apr;17(4):525-32. doi: 10.1038/ejhg.2008.203. Epub 2008 Nov 5. Eur J Hum Genet. 2009. PMID: 18985072 Free PMC article.

2

Replication of the association of the aspartic acid repeat polymorphism in the asporin gene with knee-osteoarthritis susceptibility in Han Chinese.

Jiang Q, Shi D, Yi L, Ikegawa S, Wang Y, Nakamura T, Qiao D, Liu C, Dai J. Jiang Q, et al. Among authors: qiao d. J Hum Genet. 2006;51(12):1068-1072. doi: 10.1007/s10038-006-0065-6. Epub 2006 Sep 21. J Hum Genet. 2006. PMID: 17024313

3

Cystic fibrosis transmembrane conductance regulator (CFTR) gene 5T allele may protect against prostate cancer: a case-control study in Chinese Han population.

Qiao D, Yi L, Hua L, Xu Z, Ding Y, Shi D, Ni L, Song N, Wang Y, Wu H. Qiao D, et al. J Cyst Fibros. 2008 May;7(3):210-4. doi: 10.1016/j.jcf.2007.07.011. Epub 2007 Aug 29. J Cyst Fibros. 2008. PMID: 17761461 Free article.

4

VEGF C-634G polymorphism is associated with protection from isolated ventricular septal defect: case-control and TDT studies.

Xie J, Yi L, Xu ZF, Mo XM, Hu YL, Wang DJ, Ren HZ, Han B, Wang Y, Yang C, Zhao YL, Shi DQ, Jiang YZ, Shen L, Qiao D, Chen SL, Yu BJ. Xie J, et al. Among authors: qiao d. Eur J Hum Genet. 2007 Dec;15(12):1246-51. doi: 10.1038/sj.ejhg.5201890. Epub 2007 Jul 11. Eur J Hum Genet. 2007. PMID: 17625508

5

Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax.

Ren HZ, Zhu CC, Yang C, Chen SL, Xie J, Hou YY, Xu ZF, Wang DJ, Mu DK, Ma DH, Wang Y, Ye MH, Ye ZR, Chen BF, Wang CG, Lin J, Qiao D, Yi L. Ren HZ, et al. Among authors: qiao d. Clin Genet. 2008 Aug;74(2):178-83. doi: 10.1111/j.1399-0004.2008.01030.x. Epub 2008 May 25. Clin Genet. 2008. PMID: 18505456

6

Microsatellite polymorphism in the fibrillin 3 gene and susceptibility to PCOS: a case-control study and meta-analysis.

Xie GB, Xu P, Che YN, Xia YJ, Cao YX, Wang WJ, Qiao D, Wu XK, Yi L, Gao Q, Wang Y. Xie GB, et al. Among authors: qiao d. Reprod Biomed Online. 2013 Feb;26(2):168-74. doi: 10.1016/j.rbmo.2012.10.014. Epub 2012 Oct 23. Reprod Biomed Online. 2013. PMID: 23265956

7

A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations.

Yang C, Shen L, Xu Z, Wu X, Mo X, Zhang J, Wang D, Wang Y, Peng Y, Cao L, Jiang Y, Gu H, Chen S, Bian X, Liu J, Qiao D, Yi L. Yang C, et al. Among authors: qiao d. Electrophoresis. 2009 Feb;30(3):465-71. doi: 10.1002/elps.200800321. Electrophoresis. 2009. PMID: 19145597

8

Association of DAZ1/DAZ2 deletion with spermatogenic impairment and male infertility in the South Chinese population.

Li Q, Qiao D, Song NH, Ding Y, Wang ZJ, Yang J, Wang W, Yin CJ. Li Q, et al. Among authors: qiao d. World J Urol. 2013 Dec;31(6):1403-9. doi: 10.1007/s00345-013-1058-7. Epub 2013 Mar 20. World J Urol. 2013. PMID: 23512232

9

An updated meta-analysis of XRCC4 polymorphisms and cancer risk based on 31 case-control studies.

Shao N, Jiang WY, Qiao D, Zhang SG, Wu Y, Zhang XX, Hua LX, Ding Y, Feng NH. Shao N, et al. Among authors: qiao d. Cancer Biomark. 2012-2013;12(1):37-47. doi: 10.3233/CBM-120292. Cancer Biomark. 2012. PMID: 23321468

10

[Congenital absence of the vas deferens].

Qiao D, Wu H. Qiao D, et al. Zhonghua Nan Ke Xue. 2004 Oct;10(10):775-8, 780. Zhonghua Nan Ke Xue. 2004. PMID: 15562795 Review. Chinese.

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