Clinical value of screening prenatal ultrasound combined with chromosomal microarrays in prenatal diagnosis of chromosomal abnormalities
Author:
Affiliation:
1. Department of Medical Genetics and Prenatal Diagnosis, Affiliated Maternity and Child Health Care Hospital of Nantong University, Nantong City, China
Publisher
Informa UK Limited
Link
https://www.tandfonline.com/doi/pdf/10.1080/14767058.2024.2324348
Reference35 articles.
1. The Association between the Bisphenols Residues in Amniotic Fluid and Fetal Abnormalities in Polish Pregnant Women—Its Potential Clinical Application
2. Analysis of Chromosomal Copy Number in First-Trimester Pregnancy Loss Using Next-Generation Sequencing
3. Initial Clinical Experience with NIPT for Rare Autosomal Aneuploidies and Large Copy Number Variations
4. A 6.3 Mb maternally derived microduplication of 20p13p12.2 in a fetus with Brachydactyly type D and related literature review
5. Nuchal translucency of 3.0‐3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review
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1. Chromosomal Microarray Analysis and Karyotype Analysis for Prenatal Diagnosis of Fetuses With Abnormal Ultrasound Soft Markers;Journal of Clinical Laboratory Analysis;2025-04-07
2. Clinical utility of trio whole exome sequencing in fetuses with ultrasound anomalies;Human Genomics;2025-04-05
3. Second Trimester Screening Markers of Fetal Chromosomal Abnormalities Other than Common Trisomies: A Case-Control Study;Clinical and Experimental Obstetrics & Gynecology;2024-10-21
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