| [1] |
BardosJ,HerczD,FriedenthalJ, et al. A national survey on public perceptions of miscarriage[J]. Obstet Gynecol, 2015, 125(6): 1313-1320.
|
| [2] |
ZhuJ,LiangJ,MuY, et al. Sociodemographic and obstetric characteristics of stillbirths in China: a census of nearly 4 million health facility births between 2012 and 2014[J]. Lancet Glob Health, 2016, 4(2): e109-e118.
|
| [3] |
GardnerRJM,SutherlandGR,ShafferLG. Chromosome abnormalities and genetic counseling[M].4th ed. New York: Oxford University Press, 2012.
|
| [4] |
WapnerRJ. Genetics of stillbirth[J]. Clin Obstet Gynecol, 2010, 53(3): 628-634.
|
| [5] |
LinSB,XieYJ,ChenZ, et al. Improved assay performance of single nucleotide polymorphism array over conventional karyotyping in analyzing products of conception[J]. J Chin Med Assoc, 2015, 78(7): 408-413.
|
| [6] |
王晨冉,冯碧波,翟建军. 微阵列比较基因组杂交应用于产前诊断中的研究进展[J/CD]. 中华妇幼临床医学杂志(电子版), 2014, 10(3): 393-396.
|
| [7] |
LathiRB,MassieJA,LoringM, et al. Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytogenetics[J]. PLoS One, 2012, 7(3): e31282.
|
| [8] |
American College of Obstetricians and Gynecologists Committee on Genetics. Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis[J]. Obstet Gynecol, 2013, 122(6): 1374-1377.
|
| [9] |
LevyB,SigurjonssonS,PettersenB, et al. Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis[J]. Obstet Gynecol, 2014, 124(2 Pt 1): 202-209.
|
| [10] |
WangY,ChengQ,MengL, et al. Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study[J]. Clin Genet, 2017, 91(6): 849-858.
|
| [11] |
陆国辉. 产前遗传病诊断[M]. 广州: 广东科技出版社, 2002: 245-248.
|
| [12] |
卢建,黄伟伟,李怡, 等. 染色体微阵列技术在产前诊断中的应用[J/CD]. 中国产前诊断杂志(电子版), 2016, 8(4): 8-10, 75.
|
| [13] |
曾艳,张建军. 反复妊娠21三体综合征胎儿的相关研究[J]. 中国优生与遗传杂志, 2014, 22(9): 4-6.
|
| [14] |
符梅,徐克惠. 复发性自然流产夫妇的病因分析[J/CD]. 中华妇幼临床医学杂志(电子版), 2016, 12(4): 395-400.
|
| [15] |
AntonE,VidalF,BlancoJ. Reciprocal translocations: tracing their meiotic behavior[J]. Genet Med, 2008, 10(10): 730-738.
|
| [16] |
PujolA,BenetJ,StaessenC, et al. The importance of aneuploidy screening in reciprocal translocation carriers[J]. Reproduction, 2006, 131(6): 1025-1035.
|
| [17] |
WickJB,JohnsonKJ,O′BrienJ, et al. Second-trimester diagnosis of triploidy: a series of four cases[J]. AJP Rep, 2013, 3(1): 37-40.
|
| [18] |
SchaefferAJ,ChungJ,HeretisK, et al. Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages[J]. Am J Hum Genet, 2004, 74(6): 1168-1174.
|
| [19] |
吴坚柱,何志明,林少宾, 等. 一例心脏缺陷胎儿染色体1p36.3微缺失的产前诊断[J]. 中华医学遗传学杂志, 2016, 33(3): 353-356.
|
| [20] |
周静,张硕,徐建忠, 等. 不同助孕方式中2 318例早孕期自然流产物异常核型比较[J]. 诊断学理论与实践, 2017, 16(3): 277-281.
|
| [21] |
Committee on Practice Bulletins-Obstetrics, Committee on Genetics, and the Society for Maternal-Fetal Medicine. Practice Bulletin No. 163: screening for fetal aneuploidy[J]. Obstet Gynecol, 2016, 127(5): e123-e137.
|