Jiang J - Search Results

1

[Identification of a novel mutation of the SEDL gene in X-linked spondyloepiphyseal dysplasia tarda].

Lu JF, Ma HW, Jiang J, Niu GH, Liu XM. Lu JF, et al. Among authors: jiang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Aug;21(4):309-11. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15300622 Chinese.

2

[Transmission disequilibrium test for congenital dislocation of the hip and HOXB9 gene or COL1AI gene].

Jiang J, Ma HW, Lu Y, Wang YP, Wang Y, Li QW, Ji SJ. Jiang J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Jun;20(3):193-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12778441 Chinese.

3

Gene deletion analysis of a Chinese boy with Xp21 contiguous gene deletion syndrome.

Ma HW, Jiang J, Wang YP, Wang ZC, Chen LY, Masafumi M. Ma HW, et al. Among authors: jiang j. Chin Med J (Engl). 2004 May;117(5):789-91. Chin Med J (Engl). 2004. PMID: 15161559 No abstract available.

4

[Glial fibrillary acidic protein mutation in a Chinese girl with infantile Alexander disease].

Ma HW, Lu JF, Jiang J, Chen LY, Niu GH, Wu BM, Kanazawa N, Tsujino S. Ma HW, et al. Among authors: jiang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):79-81. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696488 Chinese.

5

Mutation of acceptor splice site of the SEDL gene in X-linked spondyloepiphyseal dysplasia tarda causes the activation of cryptic splice site.

Ma HW, Jiang J, Lu JF, Guo R, Niu GH. Ma HW, et al. Among authors: jiang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):251-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952107

6

[Association analysis on the polymorphisms of PCOL2 and Sp1 binding sites of COL1A1 gene and the congenital dislocation of the hip in Chinese population].

Jiang J, Ma HW, Li QW, Lu JF, Niu GH, Zhang LJ, Ji SJ. Jiang J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):327-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952128 Chinese.

7

[The study of the correlation between the clinical phenotype of spinal muscular atrophy and SMN2 gene copy number].

Lu LP, Ma HW, Jiang J, Wang T, Hu B. Lu LP, et al. Among authors: jiang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Apr;24(2):144-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17407069 Chinese.

8

[Application of real-time PCR analysis of the SMN1gene in the carrier testing of spinal muscular atrophy].

Lu LP, Ma HW, Jiang J, Wang T, Hu B. Lu LP, et al. Among authors: jiang j. Zhongguo Dang Dai Er Ke Za Zhi. 2007 Oct;9(5):457-60. Zhongguo Dang Dai Er Ke Za Zhi. 2007. PMID: 17937858 Chinese.

9

Factors associated with early failure of the femoral neck system (FNS) in patients with femoral neck fractures.

Chen L, Jiang JB, Ma H, Duan X, Chen JL. Chen L, et al. Among authors: jiang jb. BMC Musculoskelet Disord. 2023 Nov 27;24(1):912. doi: 10.1186/s12891-023-06994-7. BMC Musculoskelet Disord. 2023. PMID: 38012667 Free PMC article.

10

[Clinical research and preliminarily exploration of genetic basis on a hereditary hemochromatosis pedigree].

Jiang J, Huang JM, Qian W, Yang L, Ye J, Hou XH. Jiang J, et al. Zhonghua Gan Zang Bing Za Zhi. 2010 Nov;18(11):842-4. doi: 10.3760/cma.j.issn.1007-3418.2010.11.012. Zhonghua Gan Zang Bing Za Zhi. 2010. PMID: 21138633 Chinese.

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