16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up

Abstract Objectives 16p13.11 microdeletion/microduplication are rare genetic diseases with incomplete penetrance, most of which have been reported in adults and children, with ultrasound phenotyping in fetuses rarely described. Here, we have analyzed prenatal ultrasound phenotypic characteristics as...

Full description

Saved in:
Bibliographic Details
Main Authors: Meiying Cai (Author), Yanting Que (Author), Xuemei Chen (Author), Yuqing Chen (Author), Bin Liang (Author), Hailong Huang (Author), Liangpu Xu (Author), Na Lin (Author)
Format: Book
Published: BMC, 2022-12-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available