Pan Q - Search Results

1

[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: pan q. 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.

2

Han Chinese population data for ten STR loci in Changsha, China.

Ma Y, Gong B, Xia J, Deng H, Pan Q, Li Q, Dai H, Wen S, Xia K. Ma Y, et al. Among authors: pan q. J Forensic Sci. 2002 Mar;47(2):404-5. J Forensic Sci. 2002. PMID: 11908620 No abstract available.

3

[Molecular cloning of the human CX 58 gene].

Lu C, Zhang H, Deng H, Xia K, Pan Q, Xia J. Lu C, et al. Among authors: pan q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Apr;19(2):95-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 11941580 Chinese.

4

Cloning of Human Myelin Protein Zero-like Genes by Bioinformatics Strategy.

Tang DS, Yu KP, Tang XX, Zhang HL, Pan Q, Dai HP, Xia JH. Tang DS, et al. Among authors: pan q. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2000;32(4):364-368. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2000. PMID: 12075424

5

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. Among authors: pan q. J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098. J Hum Genet. 2002. PMID: 12522684

6

[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: pan q. Zhonghua Yan Ke Za Zhi. 2003 Apr;39(4):206-8. Zhonghua Yan Ke Za Zhi. 2003. PMID: 12882697 Chinese.

7

[Silica nanoparticles modified as carriers for gene transfection].

Xue ZG, Zheng D, Ruan JM, Pan Q, Zhao DC, Liu XP, Chen YX, Xia JH, Xia K. Xue ZG, et al. Among authors: pan q. Yi Chuan Xue Bao. 2003 Jul;30(7):606-10. Yi Chuan Xue Bao. 2003. PMID: 14579527 Chinese.

8

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

Tang B, Zhao G, Xia K, Pan Q, Luo W, Shen L, Long Z, Dai H, Zi X, Jiang H. Tang B, et al. Among authors: pan q. Arch Neurol. 2004 Jan;61(1):49-55. doi: 10.1001/archneur.61.1.49. Arch Neurol. 2004. PMID: 14732620

9

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: pan q. Hum Genet. 2004 May;114(6):527-33. doi: 10.1007/s00439-004-1102-1. Epub 2004 Mar 12. Hum Genet. 2004. PMID: 15021985

10

[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: pan q. 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.

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