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        1.潘發明, Association between DEFB103 gene copy number variation and ankylosing spondylitis: a case–ontrol study. 

        Tissue Antigens 2.137.( 2015 July 30)

        2.張正華Genomic variations of the mevalonate pathway in porokeratosis

        Elife 9.322.( 2015 July 23)

        3.李紅SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-ssociated genes

        Genomics 2.284(2015 May 22)

        4.曹麗萍徐格林Mitochondrial DNA haplogroups and short-term neurological outcomes of ischemic stroke

        Scientific Reports 5.078(2015 May

        5.傅啟華.孫錕, A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease

        BMC Genomics4.04(2015 May 8)

        6.Liangchang Xiu, Meihua Lin, Association of DRD3, COMT, and SLC6A4 Gene Polymorphisms with Type 2 Diabetes in Southern Chinese: A Hospital-Based CaseControl Study

        Diabetes Technology & Therapeutics 2.293(2015 Apr 30)

        7.王久存,Identification and validation of the methylation biomarkers of non-small cell lung cancer (NSCLC). 

        Clinical epigenetics 6.22  2015

        8.Correlation of PCSK9 gene polymorphism with cerebral ischemic stroke in Xinjiang Han and Uygur populations
        Han D,et al.
        Med Sci Monit. 2014 Sep 30;20:1758-67. doi:10.12659/MSM.892091.
        9.A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss
        Du W, et al.
        Genomics. 2014 Aug 19. pii: S0888-7543(14)00124-4.
        10.Genetic variation in BIN1 gene and Alzheimer’s disease risk in Han Chinese individuals
        Tan MS, et al.
        Neurobiol Aging, 2014, 35(7):1781.e1-8.
        11.PRPF4 mutations cause autosomal dominant retinitis pigmentosa
        Chen X, et al.
        Hum Mol Genet, 2014, 23(11):2926-39.
        12.Clinical relevance of tag single nucleotide polymorphisms within the CAT gene in patients with PTSD in the Chongqing Han population
        Duan ZX, et al.
        Int J Clin Exp Pathol, 2014, 7(4):1724-32.
        13.The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population
        Han Y, et al.
        J Oral Pathol Med, 2014, 43(7):554-60.
        14.Gene copy number alterations in the azoospermia-associated AZFc region and their effect on spermatogenic impairment
        Lu C, et al.

        Mol Hum Reprod, 2014 online.

        15.Impacts of COX-1 gene polymorphisms on vascular outcomes in atients with ischemic stroke and treated with aspirin

        Cao L, et al.
        Gene, 2014, 546(2):172-6.
        16.Pathogenic variants screening in five non-obstructive azoospermiaassociated genes
        Lu C, et al.
        Mol Hum Reprod, 2014, 20(2):178-83.
        17.Single nucleotide polymorphisms of the interleukin-33 (IL-33) gene are associated with ankylosing spondylitis in Chinese individuals: a case–control pilot study
        Fan D, et al.
        Scand J Rheumatol, 2014, 14:1-22.
        18.Lack of Association Between TESPA1 Gene Polymorphisms (rs1801876, rs2171497, rs4758994, and rs997173) and Ankylosing Spondylitis in a Chinese Population
        Liu S, et al.
        Inflammation, 2014 online.
        19.Association between Copy Number Variations HLA-DQA1 and Ankylosing Spondylitis in Chinese Han population
        Wang J, et al.
        Genes Immun, 2013, 14(8):500-3.
        20.A1180V of Cardiac Sodium Channel Gene (SCN5A): Is It a Risk Factor for Dilated Cardiomyopathy or Just a Common Variant in Han Chinese?
        Shen C, et al.
        Dis Markers, 2013, 35(5):531-5.

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