[1] 张月萍, 伍俊萍, 李笑天, 等. 孕中期羊水细胞染色体核型分析及其异常核型发生率的比较[J]. 中华妇产科杂志,2011,46(9):644-648. [2] Gardner RJM, Sutherland GR, Shaffer LG.Chromosome abnormalities and genetic counseling[M]. New York: Oxford,2012. [3] McGowan-Jordan J, Simons A, Schmid M. ISCN2016: Aninternational system for human cytogenetic nomenclature(2016)[M]. New York: S Karger,2016. [4] Zhang Y, Zhu S, Wu J, et al.Quadrivalent asymmetry in reciprocal translocation carriers predicts meiotic segregation patterns in cleavage stage embryos[J]. Reprod Biomed Online,2014,29(4):490-498. [5] 张月萍, 朱赛娟, 刘素英, 等. 胚胎植入前诊断中多轮荧光原位杂交效果及影响因素分析[J]. 中华医学遗传学杂志,2013,30(5):522-527. [6] Mascarello JT, Hirsch B, Kearney HM, et al.Section E9 of the American College of Medical Genetics technical standards and guidelines: fluorescence in situ hybridization[J]. Genet Med,2011,13(7):667-675. [7] 荧光原位杂交技术在产前诊断中的应用协作组. 荧光原位杂交技术在产前诊断中应用的专家共识[J]. 中华妇产科杂志,2016,51(4):241-245. [8] Wapner RJ, Martin CL, Levy B, et al.Chromosomal microarray versus karyotyping for prenatal diagnosis[J]. N Engl J Med,2012,367(23):2175-2184. [9] 染色体微阵列技术在产前诊断中的应用协作组. 染色体微阵列分析技术在产前诊断中的应用专家共识[J]. 中华妇产科杂志,2014,49(8):570-572. |