Literature DB >> 30950010

[Expert consensus on the application of low-depth whole genome sequencing in prenatal diagnosis].

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Abstract

Year:  2019        PMID： 30950010     DOI： 10.3760/cma.j.issn.1003-9406.2019.04.001

Source DB:  PubMed          Journal:  Zhonghua Yi Xue Yi Chuan Xue Za Zhi        ISSN： 1003-9406


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  3 in total

1.  Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals.

Authors:  Yu Zheng; Baosheng Zhu; Jichun Tan; Yichun Guan; Cynthia C Morton; Guangxiu Lu
Journal:  Diagnostics (Basel)       Date:  2022-04-27

2.  Application of Copy Number Variation Detection to Fetal Diagnosis of Echogenic Intracardiac Focus During Pregnancy.

Authors:  Yaxian Song; Jingjing Xu; Hongmiao Li; Jiong Gao; Limin Wu; Guoping He; Wen Liu; Yue Hu; Yaqin Peng; Fang Yang; Xiaohua Jiang; Jing Wang
Journal:  Front Genet       Date:  2021-03-26       Impact factor: 4.599

3.  Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID).

Authors:  Yuxia Chen; Xiang Tang; Ling Liu; Qinrong Huang; Li Lin; Guoqing Liu; Nong Xiao
Journal:  Genes Dis       Date:  2021-12-03
  3 in total

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