Aneuploidies
-
A case of a fetus affected by complete trisomy 9 detected by noninvasive prenatal testing using cell-free DNA

-
Combined screening in the first trimester of pregnancy - how do you actually do it?

-
Fetal fraction in common aneuploidies

-
First trimester screening – combined versus ultrasound

-
Implementation of the use of fetal DNA in maternal blood for prenatal screening of aneuploidies

-
Increased nuchal translucency: the influence of maternal body mass index and weight

-
Invasive prenatal diagnostic procedures: the casuistry of a Tertiary Hospital

-
Is thickened nuchal fold more than just a second-trimester marker for Down Syndrome?

-
Monochorionic twin pregnancy with discordant karyotype

-
Performance of first-trimester combined screening for aneuploidies: impact of a contingent model implementation with cell-free fetal DNA testing

-
Prenatal diagnosis of 45, X/46, XX/46, XY chromosomal mosaicism in female fetus with Turner syndrome phenotype

-
The impact of non invasive prenatal testing (NIPT) for trisomy's in national health services (NHS) in uk on amniocentesis uptake -our experience at large university hospital in London

-
The test performance of the non-invasive prenatal test in multiple gestations and vanishing twin pregnancies

-
Trends in nuchal translucency and invasive testing

-
Triploid pregnancy: first trimester screening detection

-
Uterine fibroids and cell-free DNA screening failure

-
Why do parents refuse prenatal screening for aneuploidies?

