Prenatal diagnosis of 20p13 microdeletion syndrome

• প্রধান লেখক: Cem Yener (লেখক), Cenk Sayın (লেখক), Cihan İnan (লেখক), Hakan Gürkan (লেখক), Emine İkbal Atlı (লেখক), Engin Atlı (লেখক), Esra Altan (লেখক), Sinan Ateş (লেখক), Füsun Varol (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Elsevier, 2021-03-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: 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...