Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound-Reference-Cited by-同舟云学术

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound

Published:2018-10 Issue:5 Volume:57 Page:739-744
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Chen Chih-Ping,Chang Shu-Yuan,Chen Yen-Ni,Chern Schu-Rern,Wu Peih-Shan,Chen Shin-Wen,Lai Shih-Ting,Chuang Tzu-Yun,Yang Chien-Wen,Chen Li-Feng,Wang Wayseen

Funder

Ministry of Science and Technology

Mackay Memorial Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference40 articles.

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3. Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease;Christiansen;Circ Res,2004

4. An emerging 1q21.1 deletion-associated neurodevelopmental phenotype;Basel-Vanagaite;J Child Neurol,2011

5. Understanding the impact of 1q21.1 copy number variant;Harvard;Orphanet J Rare Dis,2011

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1. Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature;Frontiers in Genetics;2024-08-29

2. Phenotypic and genotypic characterization of 1q21.1 copy number variants: A report of 34 new individuals and literature review;American Journal of Medical Genetics Part A;2023-10-26

3. Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 1q21.1 microdeletions and microduplications;Frontiers in Medicine;2023-08-24

4. Analysis of 17 Prenatal Cases with the Chromosomal 1q21.1 Copy Number Variation;Disease Markers;2022-04-27

5. Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1;Frontiers in Genetics;2020-06-23