Xia JH - Search Results

1

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.

Tang BS, Luo W, Xia K, Xiao JF, Jiang H, Shen L, Tang JG, Zhao GH, Cai F, Pan Q, Dai HP, Yang QD, Xia JH, Evgrafov OV. Tang BS, et al. Among authors: xia k, xia jh. Hum Genet. 2004 May;114(6):527-33. doi: 10.1007/s00439-004-1102-1. Epub 2004 Mar 12. Hum Genet. 2004. PMID: 15021985

2

[A new mutation in the connexin 32 gene of a Chinese family with Charcot-Marie-Tooth disease associated with central conduction slowing].

Luo W, Tang B, Zhao G, Xia K, Yang Y, Xiao J, Yan X, Xia J. Luo W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Oct;19(5):367-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12362307 Chinese.

3

A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.

Xia J, Deng H, Feng Y, Zhang H, Pan Q, Dai H, Long Z, Tang B, Deng H, Chen Y, Zhang R, Zheng D, He Y, Xia K. Xia J, et al. J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098. J Hum Genet. 2002. PMID: 12522684

4

[Mutation analysis of neurofilament-light gene in Chinese Charcot-Marie-Tooth disease].

Luo W, Tang B, Zhao G, Li Q, Xiao J, Yang Q, Xia J. Luo W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Apr;20(2):169-70. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12673592 Chinese.

5

Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese family.

Zhang B, Xia K, Ding M, Liang D, Liu Z, Pan Q, Hu Z, Wu LQ, Cai F, Xia J. Zhang B, et al. Hum Genet. 2005 Jan;116(1-2):128-31. doi: 10.1007/s00439-004-1188-5. Epub 2004 Oct 23. Hum Genet. 2005. PMID: 15517395

6

A syndactyly type IV locus maps to 7q36.

Sato D, Liang D, Wu L, Pan Q, Xia K, Dai H, Wang H, Nishimura G, Yoshiura KI, Xia J, Niikawa N. Sato D, et al. J Hum Genet. 2007;52(6):561-564. doi: 10.1007/s10038-007-0150-5. Epub 2007 May 3. J Hum Genet. 2007. PMID: 17476456

7

Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1.

Xia JH, Yang YF, Deng H, Tang BS, Tang DS, He YG, Xia K, Chen SX, Li YX, Pan Q, Long ZG, Dai HP, Liao XD, Xiao JF, Liu ZR, Lu CY, Yu KP, Deng HX. Xia JH, et al. Among authors: xia k. J Invest Dermatol. 2000 Jun;114(6):1071-4. doi: 10.1046/j.1523-1747.2000.00978.x. J Invest Dermatol. 2000. PMID: 10844547 Free article.

8

A susceptibility locus at chromosome 3p21 linked to familial nasopharyngeal carcinoma.

Xiong W, Zeng ZY, Xia JH, Xia K, Shen SR, Li XL, Hu DX, Tan C, Xiang JJ, Zhou J, Deng H, Fan SQ, Li WF, Wang R, Zhou M, Zhu SG, Lü HB, Qian J, Zhang BC, Wang JR, Ma J, Xiao BY, Huang H, Zhang QH, Zhou YH, Luo XM, Zhou HD, Yang YX, Dai HP, Feng GY, Pan Q, Wu LQ, He L, Li GY. Xiong W, et al. Among authors: xia jh, xia k. Cancer Res. 2004 Mar 15;64(6):1972-4. doi: 10.1158/0008-5472.can-03-3253. Cancer Res. 2004. PMID: 15026332

9

[Exclusive gene mapping on retinitis pigmentosa with markers on chromosomes 3 in a Chinese kindred].

Liu Z, Deng H, Xi XH, Xia JH, Pan Q, Dai HP, Yang YJ, Deng HX, Xia K, Zheng D. Liu Z, et al. Among authors: xia jh, xia k. Zhonghua Yan Ke Za Zhi. 2003 Apr;39(4):206-8. Zhonghua Yan Ke Za Zhi. 2003. PMID: 12882697 Chinese.

10

[Chromosome analysis and phenotype location analysis on a patient with the karyotype of 45, XX, -13/46, XX, r(13)/46, XX, r(13;13)/47, XX, 2r(13)(p13q32.3)].

Liang DS, Wu LQ, Long ZG, Pan Q, Dai HP, Xia JH. Liang DS, et al. Among authors: xia jh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Aug;21(4):392-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15300643 Chinese.

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