Detection of SRY‐positive46,XX male syndrome by the analysis of cell‐free fetal DNA via non‐invasive prenatal testing
Author:
Affiliation:
1. AMES, Centro Polidiagnostico Strumentale Srl Naples Italy
2. Department of Molecular Medicine and Medical Biotechnology University of Naples "Federico II" Naples Italy
Funder
Ames Laboratory
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.2389
Reference20 articles.
1. Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing
2. Non-Invasive Prenatal Chromosomal Aneuploidy Testing - Clinical Experience: 100,000 Clinical Samples
3. Fetal Sex Chromosome Testing by Maternal Plasma DNA Sequencing
4. Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood
5. Sequencing of Circulating Cell-free DNA during Pregnancy
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Prenatal diagnosis of 46,XX testicular disorder of sex development with SRY-positive: A case report and review of the literature;European Journal of Obstetrics & Gynecology and Reproductive Biology;2023-10
2. Non-Invasive Prenatal Screening: The First Report of Pentasomy X Detected by Plasma Cell-Free DNA and Karyotype Analysis;Diagnostics;2022-06-29
3. Performance of cell-free DNA sequencing-based non-invasive prenatal testing: experience on 36,456 singleton and multiple pregnancies;BMC Medical Genomics;2021-03-30
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