SummaryObjectiveTo investigate the impact of second-trimester maternal serum screening on prenatal diagnosis of Down syndrome and the use of amniocentesis in the Taiwanese population.Materials and MethodsFrom 1990 to 2000, 166,419 amniocenteses were analyzed cytogenetically in the Taiwanese population. Among these, 58.85% were for advanced maternal age, 4.5% for abnormal ultrasound findings, 26.17% for abnormal maternal serum screening results, 1.82% for a previous child with congenital anomaly, 1.02% for a family history of chromosome aberrations, and 7.63% for other purposes. Chromosome aberrations were detected in 4,217 cases (2.53%), of which 1,277 (30.28%) were Down syndrome. Of the Down syndrome cases, 65.86% were detected by amniocen...
[[abstract]]Objective: To present our experience of amniocentesis for the prenatal diagnosis of Down...
Objective: This study investigates the performance of first- and second-trimester screening tests fo...
Down syndrome (DS) is the most common human disease caused by a structural chromosome defect. The or...
SummaryObjectiveTo investigate the impact of second-trimester maternal serum screening on prenatal d...
AbstractDown syndrome is the most common autosomal chromosome aneuploidy. The prenatal Down syndrome...
AbstractObjectiveAmniocentesis is a popular and effective prenatal diagnostic tool for chromosomal d...
SummaryObjectiveTo retrospectively investigate the 10-year experience of prenatal diagnosis of fetal...
SummaryDown syndrome (DS) is the most common human disease caused by a structural chromosome defect....
To assess the usefulness of quadruple test screening for Down syndrome in Taiwan. Materials and Meth...
AbstractObjectiveTo analyze the performance of the first trimester Down syndrome screening in a sing...
SummaryObjectiveTo assess the usefulness of quadruple test screening for Down syndrome in Taiwan.Mat...
The addition of second trimester serum markers to maternal age increases the efficacy of screening f...
A retrospective analysis of the Taiwanese National Birth Defect Registration and Notification System...
AbstractObjectiveThis study aimed to determine the rates of different fetal chromosomal abnormalitie...
A retrospective analysis of the Taiwanese National Birth Defect Registration and Notification System...
[[abstract]]Objective: To present our experience of amniocentesis for the prenatal diagnosis of Down...
Objective: This study investigates the performance of first- and second-trimester screening tests fo...
Down syndrome (DS) is the most common human disease caused by a structural chromosome defect. The or...
SummaryObjectiveTo investigate the impact of second-trimester maternal serum screening on prenatal d...
AbstractDown syndrome is the most common autosomal chromosome aneuploidy. The prenatal Down syndrome...
AbstractObjectiveAmniocentesis is a popular and effective prenatal diagnostic tool for chromosomal d...
SummaryObjectiveTo retrospectively investigate the 10-year experience of prenatal diagnosis of fetal...
SummaryDown syndrome (DS) is the most common human disease caused by a structural chromosome defect....
To assess the usefulness of quadruple test screening for Down syndrome in Taiwan. Materials and Meth...
AbstractObjectiveTo analyze the performance of the first trimester Down syndrome screening in a sing...
SummaryObjectiveTo assess the usefulness of quadruple test screening for Down syndrome in Taiwan.Mat...
The addition of second trimester serum markers to maternal age increases the efficacy of screening f...
A retrospective analysis of the Taiwanese National Birth Defect Registration and Notification System...
AbstractObjectiveThis study aimed to determine the rates of different fetal chromosomal abnormalitie...
A retrospective analysis of the Taiwanese National Birth Defect Registration and Notification System...
[[abstract]]Objective: To present our experience of amniocentesis for the prenatal diagnosis of Down...
Objective: This study investigates the performance of first- and second-trimester screening tests fo...
Down syndrome (DS) is the most common human disease caused by a structural chromosome defect. The or...