Prenatal diagnosis of 20p13 microdeletion syndrome

• Main Authors: Cem Yener (Author), Cenk Sayın (Author), Cihan İnan (Author), Hakan Gürkan (Author), Emine İkbal Atlı (Author), Engin Atlı (Author), Esra Altan (Author), Sinan Ateş (Author), Füsun Varol (Author)
• Format: Book
• Published: Elsevier, 2021-03-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Objective: The objective of this study was to report the first case of prenatal diagnosis of the fetal 20p13 microdeletion syndrome in the literature. Case report: The mother was 31 years old and had a first trimester serum screening that indicated the fetus was at low risk. The prenatal ultrasound...