Amniocentesis and Next Generation Sequencing (NGS)-Based Noninvasive Prenatal DNA Testing (NIPT) for Prenatal Diagnosis of Fetal Chromosomal Disorders-Reference-Cited by-同舟云学术

Amniocentesis and Next Generation Sequencing (NGS)-Based Noninvasive Prenatal DNA Testing (NIPT) for Prenatal Diagnosis of Fetal Chromosomal Disorders

Published:2021-05 Issue: Volume:Volume 14 Page:1811-1817
ISSN:1178-7074
Container-title:International Journal of General Medicine
language:en
Short-container-title:IJGM

Author:

Qi Qi-Ge,Tuo Ya,Liu Li-Xue,Yu Cong-Xiang,Wu Ai-Ning

Publisher

Informa UK Limited

Subject

General Medicine

Reference17 articles.

1. Enrichment of fetal and maternal long cell‐free DNA fragments from maternal plasma following DNA repair

2. Diagnosis for choroideremia in a large Chinese pedigree by next-generation sequencing (NGS) and non-invasive prenatal testing (NIPT)

3. MeDIP combined with in-solution targeted enrichment followed by NGS: Inter-individual methylation variability of fetal-specific biomarkers and their implementation in a proof of concept study for NIPT

4. Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases

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3. Assessment of Amniotic Fluid Volume in Pregnancy;RadioGraphics;2023-06-01

4. The accuracy of prenatal cell-free DNA screening for sex chromosome abnormalities: A systematic review and meta-analysis;American Journal of Obstetrics & Gynecology MFM;2023-03

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