Copy number variations of chromosome 17p11.2 region in children with development delay and in fetuses with abnormal imaging findings

Abstract Background Deletion and duplication of the 3.7 Mb region in 17p11.2 result in two syndromes, Smith-Magenis syndrome and Potocki-Lupski syndrome, which are well-known development disorders. The purpose of this study was to determine the prevalence, genetic characteristics and clinical phenot...

Full description

Saved in:
Bibliographic Details
Main Authors: Yuanyuan Zhang (Author), Xiaoliang Liu (Author), Haiming Gao (Author), Rong He (Author), Guoming Chu (Author), Yanyan Zhao (Author)
Format: Book
Published: BMC, 2021-09-01T00:00:00Z.
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