Xia JH - Search Results

1

[Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation].

Hu H, Wu LQ, Liang DS, Feng Y, Cai F, Xia K, Pan Q, Long ZG, Dai HP, Xia JH. Hu H, et al. Among authors: xia k, xia jh. Zhonghua Fu Chan Ke Za Zhi. 2005 Sep;40(9):591-4. Zhonghua Fu Chan Ke Za Zhi. 2005. PMID: 16202311 Chinese.

2

Molecular analysis of SLC26A4 gene in a Chinese deafness family.

Hu H, Liang DS, Wu LQ, Feng Y, Cai F, Xia K, Pan Q, Long ZG, Dai HP, Xia JH. Hu H, et al. Among authors: xia k, xia jh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):376-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16086271

3

Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.

Zhu HY, Wu LQ, Liang DS, Pan Q, Xia JH. Zhu HY, et al. Among authors: xia jh. Yi Chuan Xue Bao. 2006 Mar;33(3):206-12. doi: 10.1016/S0379-4172(06)60041-3. Yi Chuan Xue Bao. 2006. PMID: 16553208

4

[A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses].

Xie ZG, Hu ZM, Pan Q, Zhang RF, Liang DS, Wu LQ, Long ZG, Dai HP, Xia K, Xia JH. Xie ZG, et al. Among authors: xia k, xia jh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):147-50. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16604483 Chinese.

5

Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.

Hu H, Wu L, Feng Y, Pan Q, Long Z, Li J, Dai H, Xia K, Liang D, Niikawa N, Xia J. Hu H, et al. J Hum Genet. 2007;52(6):492-497. doi: 10.1007/s10038-007-0139-0. Epub 2007 Apr 19. J Hum Genet. 2007. PMID: 17443271

6

[Mutation screening of the dystrophin gene in 14 Chinese Duchenne/Becker muscular dystrophy patients without gross deletions].

Xue J, Zhu H, Wu L, Liang D, Pan Q, Long Z, Dai H, Xia K, Xia J. Xue J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):633-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065519 Chinese.

7

[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.

8

[A mutation IVS2+1G>A in EXT2 gene causes hereditary multiple exostoses].

Hu ZM, Zheng D, Pan Q, Yang YF, Zhao TL, Liu XP, Wu LQ, Jiang DG, Xia K, Xia JH. Hu ZM, et al. Among authors: xia k, xia jh. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Apr;21(2):97-100. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15079787 Chinese.

9

[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.

10

[Genetic diagnosis and prenatal genetic diagnosis of fragile X syndrome].

Wu LQ, Pan Q, Long ZG, Zhu JZ, Dai HP, Zheng D, Xia K, Huang XQ, Xia JH. Wu LQ, et al. Among authors: xia k, xia jh. Yi Chuan. 2003 Mar;25(2):123-8. Yi Chuan. 2003. PMID: 15639835 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

259 results

Search Page

Filters