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染色体15p+一家系细胞遗传学分析

Chromosome 15p+ family cytogenetic analysis
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摘要 目的应用荧光原位杂交技术对一家系中染色体核型为15p+的患者进行分析。方法经细胞遗传学(G显带)发现染色体核型为15p+的患者选用Yq12为探针进行荧光原位杂交。结果 15号染色体短臂的额外物质为Y染色体长臂末端的结构异染色质。结论 FISH方法可帮助确定一些未知来源染色体片段。 Objective:To analyze the chromosome karyotype of 15 p + in a family by fluorescence in situ hybridization. Methods:Patients with karyotype 15 p+ were selected by cytogenetics(G-banding)for fluorescence in situ hybridization using Yq12 as a probe. Results:The extra material of the short arm of chromosome 15 is the structural heterochromatin at the end of the long arm of the Y chromosome. Conclusion:The FISH method can help identify chromosome fragments from unknown sources.
作者 芦清霞 孙雪梅 蒋露薇 李静 LU Qing-xia;SUN Xue-mei;JIANG Lu-wei;LI Jing(Nanjing Subbo Medical Cloud Biotechnology Co.,Ltd.Nanjing Laboratory;Xinjiang Jiayin Hospital (Limited)Genetics Room)
出处 《中国优生与遗传杂志》 2018年第12期62-62,59,F0002,共3页 Chinese Journal of Birth Health & Heredity
关键词 不孕不育 荧光原位杂交 染色体 易位 Fluorescence in silu hybridization Chromosome Translocation
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  • 1Alitalo T,et al. Molecular characterization of a Y; 15 translocation seglegating in a family [ J ]. Hum Genet, 1988,79 : 29 - 35. 被引量:1
  • 2Pinton A, et al. Meiotic studies in an azoospermic boar carrying a Y ; 14 translocation [ J ]. Cytogenet Genome Res,2008,120 : 106. 被引量:1
  • 3Bajnoczky K, Meggyessy V. Coincidence of paternal 13pYq translocation and maternal increased 13p NOR activity in a child with arthrogryposis and other malformations [ J ]. Acta Paediatr Hung, 1985,26 : 151 - 156. 被引量:1
  • 4Funderburk SJ, et al. Familial Y -atttosome translocation in two unrelated girls[ J]. Ann Genet, 1982,25 : 119 - 122. 被引量:1
  • 5Ratomponirina C, Couturier J, Gabriel - Robez O, et al. Aberrations of the synaptonemal complexes in a male 46, XY, - 14, + der(14) t( Y; 14) [ J]. Ann Genet, 1985,28:214 - 218. 被引量:1
  • 6Verjaal M, Treffers PE, Nagal Y, et al. Prenatal diagnosis of a de novo Y/22 translocation [ J ]. J Med Genet, 1978,15:475 - 479. 被引量:1
  • 7Metzler - Guillcmain C, Mignon C, DepetrlsD, et al. Bivalent 15 regularly associateswith the sex vesicle in normal male meiosis[J]. Chromosome Research, 1999,7 : 369 - 378. 被引量:1
  • 8Velissarior V, Sismani C, Christopoulan S, et al. Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes : eytogenetic and molecular analysis [ J ]. Eur J Med Genet,2007,50:291 -300. 被引量:1
  • 9Kuhl H, Rottger S, Heilbronner H. Loss of the Y chromosomal PAR2 -region in four familial cases of satellited Y chromosomes (Yqs) [J]. Chromosome Res,2001,3 : 215 -222. 被引量:1
  • 10Martin Lucas M A,et al. Origin and structure of a satellited Y chrumosome[J]. Ann Genet, 1984,27 : 184 - 186. 被引量:1

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