染色体微阵列分析技术在产前遗传性疾病诊断中的价值探讨(2)
參考文献
边旭明. 实用产前诊断学[M]. 背景：人民军医出版社，2011：71
Gremer T，Landegent J， Bruckner A， et al. Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques： diagnosis of trisomy 18 with probe L1.84 [J].Hum Genet. 1986，74(4)：346-352.
梁毓，杨洋，余兰等，荧光原位杂交快速产前检测非整倍体的临床应用研究[J]。中国优生与遗传杂志。
刘慈，尹红亚，刘学军等，荧光原位杂交技术快速产前诊断胎儿常见染色体非整倍体异常研究[J]。Chinese General Practice.
Hillman SC， Pretlove S， Coomarasamy A， et al. Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis： a systematic review and meta-analysis [J]. Ultrasound Obstet Gynecol， 2011，37(1)：6-14
Lee CN， Lin SY， Lin CH， et al. Clinical utility of array comparative genomic hybridization for prenatal diagnosis： a cohort study of 3171 pregnancies [J]. BJOG，2012，119(5)：614-625
Shaffer LG， Rosenfeld JA，Dabell MP， et al. Detection of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound [J]. Prenat Diagn，2012，32(10)：986-995, http://www.100md.com(张华)
边旭明. 实用产前诊断学[M]. 背景：人民军医出版社，2011：71
Gremer T，Landegent J， Bruckner A， et al. Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques： diagnosis of trisomy 18 with probe L1.84 [J].Hum Genet. 1986，74(4)：346-352.
梁毓，杨洋，余兰等，荧光原位杂交快速产前检测非整倍体的临床应用研究[J]。中国优生与遗传杂志。
刘慈，尹红亚，刘学军等，荧光原位杂交技术快速产前诊断胎儿常见染色体非整倍体异常研究[J]。Chinese General Practice.
Hillman SC， Pretlove S， Coomarasamy A， et al. Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis： a systematic review and meta-analysis [J]. Ultrasound Obstet Gynecol， 2011，37(1)：6-14
Lee CN， Lin SY， Lin CH， et al. Clinical utility of array comparative genomic hybridization for prenatal diagnosis： a cohort study of 3171 pregnancies [J]. BJOG，2012，119(5)：614-625
Shaffer LG， Rosenfeld JA，Dabell MP， et al. Detection of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound [J]. Prenat Diagn，2012，32(10)：986-995, http://www.100md.com(张华)