Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome

Abstract Objective To share our experience on prenatal diagnosis of 7q11.23 microduplication syndrome and to further delineate the fetal phenotypes of the syndrome. Methods A retrospective study was conducted to evaluate seven cases of dup7q11.23 syndrome diagnosed prenatally by chromosomal microarr...

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Bibliographic Details
Main Authors: Yunan Wang, Chang Liu, Rong Hu, Juan Geng, Jian Lu, Xin Zhao, Ying Xiong, Jing Wu, Aihua Yin
Format: Article
Language:English
Published: BMC 2023-09-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:https://doi.org/10.1186/s13023-023-02923-y