Cargando…

Application value of NIPT for uncommon fetal chromosomal abnormalities

OBJECTIVE: To investigate the clinical value of noninvasive prenatal testing (NIPT) for fetal chromosomal deletion, duplication, and sex chromosome abnormalities. METHODS: The study included 6239 pregnant women with singletons in the first and second trimester of pregnancy who received NIPT from Dec...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yin, Lianli, Tang, Yinghua, Lu, Qing, Pan, Aiping, Shi, Mingfang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2020
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7456042/ https://www.ncbi.nlm.nih.gov/pubmed/32874204 http://dx.doi.org/10.1186/s13039-020-00508-z

Ejemplares similares

Noninvasive prenatal testing detects microdeletion abnormalities of fetal chromosome 15
por: Yin, Lianli, et al.
Publicado: (2019)

The diagnostic value of urine heat shock protein 70 and prostatic exosomal protein in chronic prostatitis
por: Tang, Yinghua, et al.
Publicado: (2021)

Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era
por: Vervecken, Evy, et al.
Publicado: (2020)

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)

The application of IL-10 and TNF-α in expressed prostatic secretions and prostatic exosomal protein in urine in the diagnosis of patients with chronic prostatitis
por: Yin, Lianli, et al.
Publicado: (2019)

Screening for Fetal Aneuploidy and Sex Chromosomal Anomalies in a Pregnant Woman With Mosaicism for Turner Syndrome—Applications and Advantages of Cell-Based NIPT
por: Jeppesen, Line Dahl, et al.
Publicado: (2021)

Failure of NIPT to detect constitutional chromoanasynthesis involving chromosome 21 in a case of fetal hydrops—A case report
por: Bone, Kathleen, et al.
Publicado: (2019)

A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC)
por: Domaradzka, Justyna, et al.
Publicado: (2021)

Comparing methods for fetal fraction determination and quality control of NIPT samples
por: van Beek, Daphne M., et al.
Publicado: (2017)

Total number of reads affects the accuracy of fetal fraction estimates in NIPT
por: Miceikaitė, Ieva, et al.
Publicado: (2021)

Regulating non-invasive prenatal testing (NIPT) for fetal sex determination
por: Taylor-Sands, Michelle, et al.
Publicado: (2023)

Amniocentesis and Next Generation Sequencing (NGS)-Based Noninvasive Prenatal DNA Testing (NIPT) for Prenatal Diagnosis of Fetal Chromosomal Disorders
por: Qi, Qi-Ge, et al.
Publicado: (2021)

Patient-friendly integrated first trimester screening by NIPT and fetal anomaly scan
por: Srebniak, Malgorzata Ilona, et al.
Publicado: (2021)

Study on the application of ultrasonography in the diagnosis of fetal cardiac structural abnormalities and the relationship between fetal cardiac structural abnormalities with chromosome abnormalities in early pregnancy
por: Ji, Xueqin, et al.
Publicado: (2021)

Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples
por: Paluoja, Priit, et al.
Publicado: (2021)

NIPT and the concerns regarding ‘routinisation’
por: Horn, Ruth
Publicado: (2022)

Fetal Calcifications Are Associated with Chromosomal Abnormalities
por: Sahlin, Ellika, et al.
Publicado: (2015)

Predicting prognosis and clinical features of the tumor microenvironment based on ferroptosis score in patients with breast cancer
por: Yin, Lianli, et al.
Publicado: (2022)

Why NIPT should be publicly funded
por: Bunnik, Eline Maria, et al.
Publicado: (2020)

More than an Incidentaloma: The Nonreportable NIPT
por: Jay, Allison M., et al.
Publicado: (2022)

Autophagy Induced by Proteasomal DUB Inhibitor NiPT Restricts NiPT-Mediated Cancer Cell Death
por: Chen, Jinghong, et al.
Publicado: (2020)

Ultrasonographic classification of 26 cases of fetal umbilical-portal-systemic venous shunts and the correlations with fetal chromosomal abnormalities
por: Lu, Lihua, et al.
Publicado: (2023)

Isodicentric Philadelphia chromosome: an uncommon chromosomal abnormality in the chronic phase of chronic myeloid leukemia (CML)
por: Loo, Eric, et al.
Publicado: (2015)

The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies
por: Li, Hongge, et al.
Publicado: (2018)

Association between fetal chromosomal abnormalities and the frequency of spontaneous abortions
por: Yang, Lan, et al.
Publicado: (2020)

What do people want to know about NIPT? Content analysis of questions emailed to national NIPT information websites
por: Tamminga, Saskia, et al.
Publicado: (2017)

Enlarged NT (≥3.5 mm) in the first trimester – not all chromosome aberrations can be detected by NIPT
por: Srebniak, Malgorzata I., et al.
Publicado: (2016)

Research on the circular RNA bioinformatics in patients with acute myocardial infarction
por: Yin, Lianli, et al.
Publicado: (2020)

An Overview of the Advances in Research on the Molecular Function and Specific Role of Circular RNA in Cardiovascular Diseases
por: Yin, Lianli, et al.
Publicado: (2022)

Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA
por: Liu, Hongtai, et al.
Publicado: (2016)

Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions
por: Kucharik, Marcel, et al.
Publicado: (2020)

Different Cutoff Values for Increased Nuchal Translucency in First-Trimester Screening to Predict Fetal Chromosomal Abnormalities
por: Su, Linjuan, et al.
Publicado: (2021)

GenomeMixer and TRUST: Novel bioinformatics tools to improve reliability of Non-Invasive Prenatal Testing (NIPT) for fetal aneuploidies
por: Pratella, David, et al.
Publicado: (2022)

Imaging single DNA molecules for high precision NIPT
por: Dahl, Fredrik, et al.
Publicado: (2018)

Non-invasive prenatal testing (NIPT): is routinization problematic?
por: Rehmann-Sutter, Christoph, et al.
Publicado: (2023)

Diagnosis of maternal Hodgkin lymphoma following abnormal findings at noninvasive prenatal screening test (NIPT): Report of two cases
por: Castellino, Alessia, et al.
Publicado: (2021)

Diagnostic Value of Chromosomal Microarray Analysis for Fetal Congenital Heart Defects with Different Cardiac Phenotypes and Extracardiac Abnormalities
por: Zhang, Simin, et al.
Publicado: (2023)

Characteristics and prognostic value of extramedullary chromosomal abnormalities in extramedullary myeloma
por: Xia, Yuan, et al.
Publicado: (2022)

Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective study
por: Sheth, Frenny J, et al.
Publicado: (2013)

Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
por: Cai, Meiying, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_p1utjqjvo566323icqf0e9b8sq