Liu JY - Search Results

1

[Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].

Wang XR, Luo RL, Dai XH, Liu JY. Wang XR, et al. Among authors: liu jy. Yi Chuan. 2007 Jul;29(7):813-6. doi: 10.1360/yc-007-0813. Yi Chuan. 2007. PMID: 17646146 Chinese.

2

Molecular genetic analysis of partial 9p trisomy in two Chinese families with mental retardation and facial anomaly.

Feng A, Dai X, Wang X, Gao Y, Luo R, Li Y, Zhang N, Liu J. Feng A, et al. J Huazhong Univ Sci Technolog Med Sci. 2011 Aug;31(4):570. doi: 10.1007/s11596-011-0492-2. Epub 2011 Aug 7. J Huazhong Univ Sci Technolog Med Sci. 2011. PMID: 21823024

3

[Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].

Liu JY, Wang XR, Zeng XL, Zhang CS, Song YC. Liu JY, et al. Yi Chuan Xue Bao. 2004 Feb;31(2):125-31. Yi Chuan Xue Bao. 2004. PMID: 15473301 Chinese.

4

[Synaptonemal complexes analysis in male fertility impairment in two men].

Liu JY, Wang XR, Zeng XL, Song YC. Liu JY, et al. Yi Chuan. 2004 Jan;26(1):13-7. Yi Chuan. 2004. PMID: 15626660 Chinese.

5

[The relationship between abnormity of synaptonemal complex and male fertility impairment in human].

Liu JY, Dai XH, Zeng XL, Zhang CS, Hao S, Song YC. Liu JY, et al. Yi Chuan. 2005 Sep;27(5):819-27. Yi Chuan. 2005. PMID: 16257917 Review. Chinese.

6

Genetic analysis of a family with 46,XY "female" associated with infertility.

Wang X, Wang XR, Liu MG, Wang Q, Liu JY. Wang X, et al. Among authors: liu mg, liu jy. Yi Chuan Xue Bao. 2006 Jan;33(1):19-25. doi: 10.1016/S0379-4172(06)60003-6. Yi Chuan Xue Bao. 2006. PMID: 16450583

7

A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33.

Dai XH, Chen WW, Wang X, Zhu QH, Li C, Li L, Liu MG, Wang QK, Liu JY. Dai XH, et al. Among authors: liu mg, liu jy. Hum Genet. 2008 Nov;124(4):423-9. doi: 10.1007/s00439-008-0566-9. Epub 2008 Oct 2. Hum Genet. 2008. PMID: 18830713

8

Identification and functional characterization of a novel splicing mutation in RP gene PRPF31.

Liu JY, Dai X, Sheng J, Cui X, Wang X, Jiang X, Tu X, Tang Z, Bai Y, Liu M, Wang QK. Liu JY, et al. Among authors: liu m. Biochem Biophys Res Commun. 2008 Mar 7;367(2):420-6. doi: 10.1016/j.bbrc.2007.12.156. Epub 2008 Jan 3. Biochem Biophys Res Commun. 2008. PMID: 18177735 Free PMC article.

9

Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation.

Liu JY, Ren X, Yang X, Guo T, Yao Q, Li L, Dai X, Zhang M, Wang L, Liu M, Wang QK. Liu JY, et al. Among authors: liu m. J Hum Genet. 2007;52(6):565-570. doi: 10.1007/s10038-007-0152-3. Epub 2007 May 22. J Hum Genet. 2007. PMID: 17516023

10

Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification.

Dai X, Gao Y, Xu Z, Cui X, Liu J, Li Y, Xu H, Liu M, Wang QK, Liu JY. Dai X, et al. Among authors: liu j, liu m, liu jy. Am J Med Genet B Neuropsychiatr Genet. 2010 Oct 5;153B(7):1305-10. doi: 10.1002/ajmg.b.31102. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20552677

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