期刊文献+

新疆汉族和维吾尔族群体5个X-STR基因座的遗传多态性

下载PDF
导出
摘要 近年来X染色体STR(X—STR)已得到法医工作者的青睐,与常染色体STR联合应用于法医学实践。X—STR与常染色体STR相比有其独特的特征同,遗传过程中母亲的X染色体可以遗传给女儿和儿子,而父亲的X染色体只能遗传给女儿。由于单个X—STR提供的信息有限,因此有必要寻找更多多态性高的X—STR基因座并建立群体遗传学资料。
出处 《法医学杂志》 CAS CSCD 2010年第2期137-139,共3页 Journal of Forensic Medicine
  • 相关文献

参考文献12

  • 1吕德坚,陈树春,王学文,刘秋玲,陆惠玲.广东汉族DXS10011和DXS8377单体型[J].法医学杂志,2006,22(3):207-209. 被引量:2
  • 2金洁,吴朝阳,刘木根,盛瑞兰,陆化,朱广荣,许文林.中国汉族人群DXS15位点多态性研究及其应用[J].复旦学报(医学版),2002,29(1):50-52. 被引量:22
  • 3Poetseh M,Petersmann H,Repenning A,et al.Development of two pentaplex systems with X-chromosomal STR loci and their allele frequencies in a northeast German population[J].Forensic Sci Int,2005,155 (1):71-76.
  • 4高雅,金天博,余兵,杜宏,李生斌.藏族X染色体10个STR位点的遗传多态性[J].中华医学遗传学杂志,2006,23(1):97-99. 被引量:16
  • 5Szibor R,Hering S,Edelmann J.A new Web site compiling forensic chromosome X research is now online[J].Int J Legal Med,2006,120(4):252-254.
  • 6Szibor R,Krawczak M,Hering S,et al.Use of Xlinked markers for forensic purposes[J].Int J Legal Med,2003,117(2):67-74.
  • 7Deng JQ,Ying BW,Shi MS,et al.Two X-chromosome STR loci DXS6804 and DXS9896 frequency data in Chinese population[J].J Forensic Sci,2003,48(4):886.
  • 8Shi MS,Deng JQ,Ying BW,et al.Two X-chromosome STR loci DXS6807 and DXS7133 frequency data in Chinese population[J].J Forensic Sci,2003,48(3):689.
  • 9Liu QL,Lv D J,Wu XL,et al.Development of a five ChX STRs loci typing system[J].Int J Legal Med,2008,122 (3):261-265.
  • 10Desmarais D,Zhong Y,Chakraborty R,et al.Development of a highly polymorphic STR marker for identity testing purposes at the human androgen receptor gene (HUMARA)[J].J Forensic Sci,1998,43 (5):1046 -1049.

二级参考文献24

  • 1吕德坚,刘秋玲.X染色体STR的法医学应用进展[J].中国法医学杂志,2002,17(4):252-255. 被引量:33
  • 2刘秋玲,吕德坚,崔崴.3个X染色体短串联重复的复合扩增及其多态性[J].中华医学遗传学杂志,2004,21(3):233-235. 被引量:5
  • 3应斌武,石美森,邓建强,李英碧,吴谨,颜静,张霁,侯一平.DXS6804/DXS9896/GATA144D04基因座在中国汉族群体中的遗传多态性及其法医学应用[J].遗传,2004,26(5):603-606. 被引量:15
  • 4Gitschier J,Wood WI,Goralka TM, et al. Characterization of human factor Ⅷ gene. Nature, 1984,312: 326
  • 5Pemberton S, Lindley P,Zaitsev V, et al. A molecular model for the triplicated a domains of human factor Ⅷ based on the crystal structure of human ceruloplasmin. Blood, 1997,89 (7): 2413
  • 6Pieneman WC, Deutz-Terlouco PP, Reitsma PH, et al.,Scre n for mutations in hemophilia A pations by multiplex PCR-SSCP, Southen blotting and RNA analysis: the detection of a genetic abnormality in the factor Ⅷ gene in 30 out of 35 pations. British Journl of Haematology, 1995,90: 442
  • 7Dib C, Faure S,Fizames C, et al. A comprehesive senetic map of the human genome based on 5264 microsatellites. Nature, 1996,38:132
  • 8Nei M,Roychoudhury AK.Sampling variances of heterozygosity and genetic distance.Genetics,1974,76:379-390.
  • 9Botstein D,White RI,Skolnich M,et al.Construction of a genetic linkage map in man using restriction fragment length polymorphisms.Am J Hum Genet,1980,32:314-331.
  • 10Desmarais D,Zhong Y,Chakraborty R,et al.Development of a highly polymorphic STR marker for identity testing purposes at the human androgen receptor gene (HUMARA).J Forensic Sci,1998,43:1046-1049.

共引文献36

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部