Genomics‐based non‐invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women
M Badeau, C Lindsay, J Blais… - Cochrane Database …, 2017 - cochranelibrary.com
Background Common fetal aneuploidies include Down syndrome (trisomy 21 or T21),
Edward syndrome (trisomy 18 or T18), Patau syndrome (trisomy 13 or T13), Turner …
Edward syndrome (trisomy 18 or T18), Patau syndrome (trisomy 13 or T13), Turner …
[HTML][HTML] Genome-wide analysis of Epstein-Barr virus (EBV) integration and strain in C666-1 and Raji cells
K Xiao, Z Yu, X Li, X Li, K Tang, C Tu, P Qi… - Journal of …, 2016 - ncbi.nlm.nih.gov
EBV is a key risk factor for many malignancy diseases such as nasopharyngeal carcinoma
(NPC) and Burkitt lymphoma (BL). EBV integration has been reported, but its scale and …
(NPC) and Burkitt lymphoma (BL). EBV integration has been reported, but its scale and …
Clinical calculator based on CT and clinicopathologic characteristics predicts short-term prognosis following resection of microsatellite-stabilized diffuse gastric cancer
P Liu, P Ding, H Guo, J Yang, H Wu, J Wu, P Yang… - Abdominal …, 2024 - Springer
Purpose Although microsatellite stability/Epithelial-mesenchymal transition (MSS/EMT)
subtypes have been reported in multiple cancer prognosis studies, strong confounding …
subtypes have been reported in multiple cancer prognosis studies, strong confounding …
Disorder of sexual development males with XYY in blood have exactly X/XY/XYY mosaicism in gonad tissues
Y Yang, F Chen, Z Luo, Y Zheng, J Zheng, Y Fu… - Frontiers in …, 2021 - frontiersin.org
Y chromosome represents masculinization. The extra Y chromosome of XYY patients
usually leads to over-masculinization phenotypes. The occurrence of several DSD cases …
usually leads to over-masculinization phenotypes. The occurrence of several DSD cases …
Validation of two‐channel sequencing‐by‐synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations
K Neveling, D Tjwan Thung, L Beulen… - Prenatal …, 2016 - Wiley Online Library
Abstract Objective To validate Illumina's two‐channel NextSeq 500 sequencing system for
noninvasive prenatal testing (NIPT) of fetal whole chromosome and partial aberrations …
noninvasive prenatal testing (NIPT) of fetal whole chromosome and partial aberrations …
A non-invasive prenatal test with accurate fetal fraction measurement
The present disclosure relates to methods for non-invasive prenatal testing (NIPT) using
semm from a maternal blood sample taken during pregnancy. The methods provide efficient …
semm from a maternal blood sample taken during pregnancy. The methods provide efficient …