A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease

被引：0
|
作者：
Xiaoqing Zhang
Yuejuan Xu
Deyuan Liu
Juan Geng
Sun Chen
Zhengwen Jiang
Qihua Fu
Kun Sun
机构：
[1] Shanghai Jiao Tong University School of Medicine,Department of Laboratory Medicine, Shanghai Children’s Medical Center
[2] Shanghai Jiao Tong University School of Medicine,Department of Pediatric Cardiology, Xinhua Hospital
[3] Genesky Diagnostics (Suzhou) Inc,undefined
来源：
BMC Genomics | / 16卷
关键词：
Copy number variation; 22q11.2 deletion; Congenital heart disease; Multiplex ligation-dependent probe amplification;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [1] A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease
    Zhang, Xiaoqing
    Xu, Yuejuan
    Liu, Deyuan
    Geng, Juan
    Chen, Sun
    Jiang, Zhengwen
    Fu, Qihua
    Sun, Kun
    BMC GENOMICS, 2015, 16
  • [2] A novel method based on multiplex ligation-dependent probe amplification for the detection of 22q112 copy number variations in patients with congenital heart diseases
    Zhang, X.
    CLINICAL BIOCHEMISTRY, 2014, 47 (09) : 783 - 784
  • [3] Analysis of gene copy number variations in patients with congenital heart disease using multiplex ligation-dependent probe amplification
    Mutlu, Esra Tuba
    Aykan, Hayrettin Hakan
    Karagoz, Tevfik
    ANATOLIAN JOURNAL OF CARDIOLOGY, 2018, 20 (01): : 9 - 15
  • [4] Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases
    Nagy, Orsolya
    Szakszon, Katalin
    Biro, Brigitta Orsolya
    Mogyorosy, Gabor
    Nagy, Dora
    Nagy, Bailin
    Balogh, Istvan
    Ujfalusi, Aniko
    JOURNAL OF BIOTECHNOLOGY, 2019, 299 : 86 - 95
  • [5] Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases
    Nagy, O.
    Szakszon, K.
    Nagy, D.
    Mogyorosy, G.
    Biro, B.
    Nagy, B.
    Balogh, I.
    Ujfalusi, A.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1312 - 1313
  • [6] Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect
    Jingjing Zhang
    Dingyuan Ma
    Yan Wang
    Li Cao
    Yun Wu
    Fengchang Qiao
    An Liu
    Li Li
    Ying Lin
    Gang Liu
    Cuiyun Liu
    Ping Hu
    Zhengfeng Xu
    Molecular Cytogenetics, 8
  • [7] Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect
    Zhang, Jingjing
    Ma, Dingyuan
    Wang, Yan
    Cao, Li
    Wu, Yun
    Qiao, Fengchang
    Liu, An
    Li, Li
    Lin, Ying
    Liu, Gang
    Liu, Cuiyun
    Hu, Ping
    Xu, Zhengfeng
    MOLECULAR CYTOGENETICS, 2015, 8
  • [8] Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart disease
    Guida, Valentina
    Lepri, Francesca
    Vijzelaar, Raymon
    De Zorzi, Andrea
    Versacci, Paolo
    Digilio, Maria Cristina
    Marino, Bruno
    De Luca, Alessandro
    Dallapiccola, Bruno
    DISEASE MARKERS, 2010, 28 (05) : 287 - 292
  • [9] A Pilot Study of Multiplex Ligation-Dependent Probe Amplification Evaluation of Copy Number Variations in Romanian Children with Congenital Heart Defects
    Bolundut, Alexandru Cristian
    Nazarie, Florina
    Lazea, Cecilia
    Sufana, Crina
    Miclea, Diana
    Lazar, Calin
    Mihu, Carmen Mihaela
    GENES, 2024, 15 (02)
  • [10] Identification of clinical features to predict 22q11.2 deletion syndrome, proven by multiplex ligation-dependent probe amplification
    Rojnueangnit, K.
    Khetkham, T.
    Onsod, P.
    Chareonsirisuthigul, T.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 902 - 902
12345