Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication-Reference-Cited by-同舟云学术

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Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication

Published:2017-04 Issue:4 Volume:19 Page:e2948
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J Gene Med

Author:

Wang Hong-Dan¹,Liu Lin²,Wu Dong¹,Li Tao¹,Cui Cun-Ying²,Zhang Lian-Zhong²,Wang Cheng-Zeng³

Affiliation:

1. Institute of Medical Genetics, Henan Provincial People's Hospital; Zhengzhou University People's Hospital; Zhengzhou China

2. Department of Cardiovascular Ultrasound, Henan Provincial People's Hospital; Zhengzhou University People's Hospital; Zhengzhou China

3. Department of Ultrasound, the Affiliated Cancer Hospital; Zhengzhou University; Zhengzhou China

Funder

National Natural Science Foundation of China

Henan Provincial Health System

Tackle Key Problems in Science and Technology

Publisher

Wiley

Subject

Genetics(clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Reference30 articles.

1. Phenotypic variability associated with a large recurrent 1q21.1 microduplication in a three-generation family;Verhagen;Mol Syndromol,2015

2. 1q21.1 microduplication expression in adults;Dolcetti;Genet Med,2013

3. Clinical phenotype of the recurrent 1q21.1 copy-number variant;Bernier;Genet Med,2016

4. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities;Brunetti-Pierri;Nat Genet,2008

5. Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes;Mefford;N Engl J Med,2008

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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. Chromosomal microarray testing yield in 829 cases of microcephaly: a clinical characteristics-based analysis for prenatal and postnatal cases;Archives of Gynecology and Obstetrics;2024-03-18

3. 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

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

5. Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study;BMC Medical Genomics;2023-08-23

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