Liu QJ - Search Results

1

[Fine mapping of Smith-Fineman-Myers syndrome and exclusion of GPC3, GPCR2 MST4 and GLUD2 as candidate genes].

Liu QJ, Gong YQ, Li JX, Zhang XY, Gao GM, Guo YS. Liu QJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):198-202. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15192816 Chinese.

2

[Linkage analysis of X-linked nuclear protein gene in Smith-Fineman-Myers syndrome].

Liu Q, Gong Y, Chen B, Guo C, Li J, Guo Y. Liu Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Feb;19(1):22-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 11836680 Chinese.

3

[The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].

Guo C, Guo Q, Gong Y, Chen B, Liu Q, Li J, Gao G, Zhou H. Guo C, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Aug;19(4):295-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12170465 Chinese.

4

[Polymorphic loci and polymorphism analysis of short tandem repeats within XNP gene].

Liu QJ, Gong YQ, Guo CH, Chen BX, Li JX, Guo YS. Liu QJ, et al. Yi Chuan Xue Bao. 2002;29(3):201-5. Yi Chuan Xue Bao. 2002. PMID: 12182071 Chinese.

5

[Genomic structure of low density lipoprotein receptor related protein 5 gene].

Li J, Gong Y, Liu Q, Chen B, Guo C, Guo Y. Li J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Dec;19(6):467-70. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12476416 Chinese.

6

[Application of homozygosity mapping to the fine mapping of the osteoporosis-pseudoglioma syndrome locus].

Gong YQ, Li JX, Liu QJ, Chen BX, Guo CH, Gao GM. Gong YQ, et al. Among authors: liu qj. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Feb;20(1):53-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12579502 Chinese.

7

[Gene mapping of a nonsyndromic hearing impairmint family].

Cheng L, Gong Y, Liu Q, Chen B, Guo C, Li J, Zhang X, Lu Y, Gao G, Zhou H, Guo Y. Cheng L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Apr;20(2):89-93. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12673573 Chinese.

8

A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads.

Lu Y, Guo C, Liu Q, Zhang X, Cheng L, Li J, Chen B, Gao G, Zhou H, Guo Y, Li Y, Gong Y. Lu Y, et al. Am J Med Genet A. 2003 Jul 30;120A(3):345-9. doi: 10.1002/ajmg.a.20090. Am J Med Genet A. 2003. PMID: 12838553

9

A locus for nonspecific X-linked mental retardation mapped to a 22.3 cM region of Xp11.3-q22.3.

Zhang X, Liu Q, Chen B, Guo C, Li J, Gao G, Guo Y, Gong Y. Zhang X, et al. Am J Med Genet A. 2004 Sep 1;129A(3):286-9. doi: 10.1002/ajmg.a.30121. Am J Med Genet A. 2004. PMID: 15326629

10

[Characterization of genomic structure and mutation analysis of SMARCA1 gene in a Smith-Fineman-Myers syndrome family].

Liu QJ, Gong YQ, Zhang XY, Gao GM, Guo YS. Liu QJ, et al. Yi Chuan Xue Bao. 2004 Feb;31(2):114-8. Yi Chuan Xue Bao. 2004. PMID: 15473299 Chinese.

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