换一批
换一批Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.
第一作者：
Min,Pan
第一单位：
Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China.
作者：
主题词
成年人(Adult);非整倍性(Aneuploidy);绒毛膜绒毛取样(Chorionic Villi Sampling);染色体畸变(Chromosome Aberrations);染色体障碍(Chromosome Disorders);染色体, 人, 13对(Chromosomes, Human, Pair 13);染色体, 人, 18对(Chromosomes, Human, Pair 18);队列研究(Cohort Studies);DNA拷贝数变异(DNA Copy Number Variations);唐氏综合征(Down Syndrome);女(雌)性(Female);荧光(Fluorescence);人类(Humans);核型分析(Karyotyping);Klinefelter综合征(Klinefelter Syndrome);颈部透明带检查(Nuchal Translucency Measurement);寡核苷酸序列分析(Oligonucleotide Array Sequence Analysis);聚合酶链反应(Polymerase Chain Reaction);妊娠(Pregnancy);产前诊断(Prenatal Diagnosis);回顾性研究(Retrospective Studies);三体性(Trisomy);特纳综合征(Turner Syndrome);青年人(Young Adult)
DOI
10.1016/j.ejogrb.2015.12.024
PMID
26771907
发布时间
2022-04-09
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