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罗伯逊易位致少精子症4例报告 被引量:1

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摘要 染色体结构异常是导致自然流产、畸形儿、死胎、不育等的遗传因素之一,罗伯逊易位是主要的结构异常,总体发生频率约为1/1000新生儿[1],罗伯逊易位患者大部分由于习惯性流产、不育等才被发现。本文就4例罗伯逊易位患者资料结合文献加以分析,报告如下。
出处 《中华男科学杂志》 CAS CSCD 北大核心 2011年第2期170-172,共3页 National Journal of Andrology
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参考文献16

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  • 4Ogur G, Van Assche E, Vegetti W, et al. Chromosomal segrega- tion in spermatozoa of 14 Robertsonian translocation carriers. Mol Hum Reprod, 2006, 12(3): 209-215. 被引量:1
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二级参考文献10

  • 1Estop AM,Cieply K,Aston CE.The meiotic segregation pattern of a reciprocal translocation t(10;12)(q26.1;p13.3)by fluorescent in situ hybridization sperm analysis[J].Eur J Hum Genet,1997, 6(2) :78-82. 被引量:1
  • 2Stern C,Pertile M,Norris H,et al.Chromosome translocations in couples with in-vitro fertilization implantation failure[J].Hum Reprod,1999,14(8):2097-2101. 被引量:1
  • 3Martini E,Coonen E,Bergh A,et al.Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3)by triple FISH[J].Hum Genet,1998,102(2):157-165. 被引量:1
  • 4刘权章主编.人类染色体方法学[M].北京:人民卫生出版社,1990.139-140 被引量:1
  • 5Van Hummelen P,Manchester D,Lowe X,et al.Meiotic segregation,recombination,and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3)reciprocal translocation carrier by three-and four-probe multicolor FISH in sperm[J].Am J Hum Genet,1997,61(3):651-659. 被引量:1
  • 6Rives N,Jarnot M,Mousset-Simeon N,et al.Fluorescence in situ hybridisation(FISH)analysis of chromosome segregation and interchromosomal effect in spermatozoa of a reciprocal translocation t(9,10)(q11;p11.1)carrier[J].Hum Genet,2003,48(10):535-540. 被引量:1
  • 7Hatakeyama C,Gao H,Harmer K,et al.Meiotic segregation patterns and ICSI pregnancy outcome of a rare(13;21)Robertsonian translocation carrier:a case report[J].Hum Reprod,2006,21(4):976-979. 被引量:1
  • 8彭惠民,唐吟宇,郭玉萍,张静.异常核型者的Ag-NOR和Ag-AA分析[J].中国优生与遗传杂志,2000,8(2):40-41. 被引量:2
  • 9张淑凤,王为娜,王绍荣.二胎生育优生监护的研究[J].中国优生与遗传杂志,2000,8(3):125-126. 被引量:1
  • 10刘永章,竺海波.用双色荧光原位杂交技术检测罗伯逊易位携带者的精子染色体[J].中华男科学杂志,2004,10(2):90-93. 被引量:5

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