Cargando…
Whole genome non-invasive prenatal testing in prenatal screening algorithm: clinical experience from 12,700 pregnancies
BACKGROUND: A fast adoption of a non–invasive prenatal testing (NIPT) in clinical practice is a global tendency last years. Firstly, in Russia according a new regulation it was possible to perform a widescale testing of pregnant women in chromosomal abnormality risk. The aim of the study—to assess e...
Autores principales: | Baranova, Elena E., Sagaydak, Olesya V., Galaktionova, Alexandra M., Kuznetsova, Ekaterina S., Kaplanova, Madina T., Makarova, Maria V., Belenikin, Maxim S., Olenev, Anton S., Songolova, Ekaterina N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364619/ https://www.ncbi.nlm.nih.gov/pubmed/35945516 http://dx.doi.org/10.1186/s12884-022-04966-8 |
Ejemplares similares
-
The CFTR Gene Germline Heterozygous Pathogenic Variants in Russian Patients with Malignant Neoplasms and Healthy Carriers: 11,800 WGS Results
por: Makarova, Maria, et al.
Publicado: (2023) -
A Unique Observation of a Patient with Vulto-van Silfhout-de Vries Syndrome
por: Bodunova, Natalia, et al.
Publicado: (2022) -
Diagnosis of Menke‐Hennekam syndrome by prenatal whole exome sequencing and review of prenatal signs
por: Cogan, Guillaume, et al.
Publicado: (2023) -
Transferability of the PRS estimates for height and BMI obtained from the European ethnic groups to the Western Russian populations
por: Albert, E. A., et al.
Publicado: (2023) -
Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies—Experience from a Local Prenatal Diagnostic Laboratory
por: Lai, Theodora Hei Tung, et al.
Publicado: (2022)