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qi fang lin
(6 results)?
Prevalence of migraine in Han Chinese of Fujian province: An epidemiological study.
Medicine (Baltimore). 2018 Dec;97(52):e13500. doi: 10.1097/MD.0000000000013500.
Medicine (Baltimore). 2018.
PMID: 30593125
Free PMC article.
Association of genetic loci for migraine susceptibility in the she people of China.
Lin QF, Fu XG, Yao LT, Yang J, Cao LY, Xin YT, Hou JX, Ye LF, Huang GB.
Lin QF, et al.
J Headache Pain. 2015;16:553. doi: 10.1186/s10194-015-0553-1. Epub 2015 Aug 1.
J Headache Pain. 2015.
PMID: 26231841
Free PMC article.
Item in Clipboard
Association between PRDM16, MEF2D, TRPM8, LRP1 gene polymorphisms and migraine susceptibility in the She ethnic population in China.
Fu X, Yang J, Wu X, Lin Q, Zeng Y, Xia Q, Cao L, Huang B, Huang G.
Fu X, et al. Among authors: lin q.
Clin Invest Med. 2019 Mar 23;42(1):E21-E30. doi: 10.25011/cim.v42i1.32389.
Clin Invest Med. 2019.
PMID: 30904033
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Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.
He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N, Chen WJ.
He J, et al.
Gene. 2013 Apr 15;518(2):325-9. doi: 10.1016/j.gene.2012.12.109. Epub 2013 Jan 23.
Gene. 2013.
PMID: 23352792
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Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China.
Cai J, Lin Y, Chen W, Lin Q, Cai B, Wang N, Zheng W.
Cai J, et al. Among authors: lin q.
Neurol Sci. 2013 Nov;34(11):2001-6. doi: 10.1007/s10072-013-1436-3. Epub 2013 Apr 30.
Neurol Sci. 2013.
PMID: 23624603
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Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.
Chen WJ, Lin QF, Zhang QJ, He J, Liu XY, Lin MT, Murong SX, Liou CW, Wang N.
Chen WJ, et al.
Clin Chim Acta. 2013 Aug 23;423:35-8. doi: 10.1016/j.cca.2013.04.006. Epub 2013 Apr 13.
Clin Chim Acta. 2013.
PMID: 23588064
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Modification of phenotype by SMN2 copy numbers in two Chinese families with SMN1 deletion in two continuous generations.
Chen WJ, He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N.
Chen WJ, et al.
Clin Chim Acta. 2012 Nov 20;413(23-24):1855-60. doi: 10.1016/j.cca.2012.07.020. Epub 2012 Aug 4.
Clin Chim Acta. 2012.
PMID: 22884440
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