Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses
Author:
Affiliation:
1. Faculty of Medicine, Department of Medical Genetics and
2. Faculty of Medicine, Department of Obstetrics and Gynecology, Gazi University, Ankara, Turkey
Publisher
Informa UK Limited
Subject
Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/14767058.2016.1214700
Reference10 articles.
1. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism
2. Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction
3. Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony
4. Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and molecular genetic analysis
5. A case of mosaic trisomy 2 diagnosed at amniocentesis in an abnormal fetus and confirmed in multiple fetal tissues
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2. Prenatal Detection of Trisomy 2: Considerations for Genetic Counseling and Testing;Genes;2023-04-14
3. Pregnancies with trisomy 2 cells in chorionic villi: Ultrasound determines the outcome;European Journal of Obstetrics & Gynecology and Reproductive Biology;2021-06
4. Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis;Genetic Disorders and the Fetus;2021-04-20
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