Fetal Genetic Diagnosis by Chorionic Villus Sampling: Evaluation of the Five-Year Experience from a Single Center
Author:
Affiliation:
1. Obstetrics and Gynecology Department, Ministry of Health Ankara City Hospital, Ankara, Turkey
2. Department of Medical Genetics, Ministry of Health Ankara City Hospital, Ankara, Turkey
Publisher
Informa UK Limited
Subject
General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/15513815.2019.1707919
Reference30 articles.
1. Prenatal invasive testing: a 13-year single institution experience
2. Changes in and Efficacies of Indications for Invasive Prenatal Diagnosis of Cytogenomic Abnormalities: 13 Years of Experience in a Single Center
3. Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population
4. ACOG Practice Bulletin No. 88: Invasive Prenatal Testing for Aneuploidy
5. Feasibility, accuracy and safety of chorionic villus sampling: a report of 10 741 cases
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1. Advancements of non-invasive prenatal testing: the role of obstetricians;Frontiers in Medicine;2024-06-13
2. Evaluation of fetal and maternal outcomes in chorion villus sampling (CVS);Advanced Biomedical Research;2023
3. A Multi-centre Experience of Trans-abdominal Chorionic Villus Sampling in Pakistan;Journal of the College of Physicians and Surgeons Pakistan;2023-01-01
4. Complementary Approaches in Fetal Genetic Diagnosis: Decision-Making Process and Alternative Choices for Clinicians in a Secondary Health Care Institution;Fetal and Pediatric Pathology;2022-01-03
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