Cargando…
Enlarged NT (≥3.5 mm) in the first trimester – not all chromosome aberrations can be detected by NIPT
BACKGROUND: Since non-invasive prenatal testing (NIPT) in maternal blood became available, we evaluated which chromosome aberrations found in our cohort of fetuses with an enlarged NT in the first trimester of pregnancy (tested with SNP microarray) could be detected by NIPT as well. METHOD: 362 fetu...
Autores principales: | Srebniak, Malgorzata I., de Wit, Merel C., Diderich, Karin E. M., Govaerts, Lutgarde C. P., Joosten, Marieke, Knapen, Maarten F. C. M., Bos, Marnix J., Looye-Bruinsma, Gerda A. G., Koningen, Mieke, Go, Attie T. J. I., Galjaard, Robert Jan H., Van Opstal, Diane |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015200/ https://www.ncbi.nlm.nih.gov/pubmed/27610202 http://dx.doi.org/10.1186/s13039-016-0279-z |
Ejemplares similares
-
Patient-friendly integrated first trimester screening by NIPT and fetal anomaly scan
por: Srebniak, Malgorzata Ilona, et al.
Publicado: (2021) -
Social and medical need for whole genome high resolution NIPT
por: Srebniak, Malgorzata I., et al.
Publicado: (2019) -
False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review
por: Van Opstal, Diane, et al.
Publicado: (2016) -
Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?
por: Diderich, Karin, et al.
Publicado: (2019) -
Placental studies elucidate discrepancies between NIPT showing a structural chromosome aberration and a differently abnormal fetal karyotype
por: Van Opstal, Diane, et al.
Publicado: (2019)