Polar body biopsy and aneuploidy testing by simultaneous detection of six chromosomes
Isolated right diaphragmatic eventration mimicking congenital heart disease in utero
Prenatal diagnosis of de novo (7;19)(q11.2;q13.3) translocation associated with a thick corpus callosum and Wilms tumor of the kidneys
Prenatal diagnosis of Beckwith-Wiedemann syndrome
Estimating the attitude of immigrants toward primary prevention of the hemoglobinopathies
Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro
First-trimester screening for Down syndrome with ductus venosus Doppler studies in addition to nuchal translucency and serum markers
Second trimester ultrasound prenasal thickness combined with nasal bone length
A semi-quantitative microarray method to detect fetal RNAs in maternal plasma
Aneuploidy screening in coelomic samples using fluorescence in situ hybridisation (FISH)
The influence of maternal insulin-dependent diabetes on fetal nuchal translucency thickness and first-trimester maternal serum biochemical markers of aneuploidy
Prenatal diagnosis in a family with X-linked hydrocephalus
Trisomy 2 due to a 3
Prenatal infantile cortical hyperostosis (Caffey's disease)
Prenatal diagnosis of del(9)(p24)
Prediction of pregnancy complications by first-trimester maternal serum PAPP-A and free β -hCG and with second-trimester uterine artery Doppler
Interstitial deletion del(10)(q25.2q25.3 ˜ 26.11)—case report and review of the literature
Uterine lavage in prenatal screening for aneuploidy in continuing pregnancies
Contingent screening for Down syndrome
Prenatal diagnosis of partial trisomy 16q and distal 22q13 deletion associated with dolichocephaly and frontal bossing on second-trimester ultrasound
Second-trimester diagnosis of trisomy 9 associated with abnormal maternal serum screening results
Apparently low maternal serum inhibin A levels in second-trimester screening
Prenatally diagnosed mosaic trisomy 17
Current awareness in prenatal diagnosis