Publications by authors named "Lique Du"

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Clinical diagnosis of genetic disorders at both single-nucleotide and chromosomal levels based on BGISEQ-500 platform.
Yanqiu Liu, Liangwei Mao, Hui Huang, Wei Li, Jianfen Man, Lique Du

Hum Genome Var· May 2023

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A Novel CNGA1 Gene Mutation (c.G622A) of Autosomal Recessive Retinitis Pigmentosa Leads to the CNGA1 Protein Reduction on Membrane.
Qing Gao, Yifan Liu, Xinlan Lei, Qinqin Deng, Yongqing Tong, Lique Du

Biochem Genet· August 2019

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Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform.
Yan Sun, Jing Yuan, Limin Wu, Min Li, Xiaoli Cui, Lique Du

Medicine (Baltimore)· March 2019

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Targeted next-generation sequencing as a comprehensive test for Mendelian diseases: a cohort diagnostic study.
Yan Sun, Jianfen Man, Yang Wan, Gao Pan, Lique Du

Sci Rep· August 2018

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Identification of a Disease-Causing Mutation in a Chinese Patient with Retinitis Pigmentosa by Targeted Next-Generation Sequencing.
Jianping Xiao, Xueqin Guo, Yong Wang, Mingkun Shao, Xiaoming Wei, Lique Du

Eur J Ophthalmol· November 2017

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Targeted Next-Generation Sequencing for Clinical Diagnosis of 561 Mendelian Diseases.
Yanqiu Liu, Xiaoming Wei, Xiangdong Kong, Xueqin Guo, Yan Sun, Lique Du

PLoS One· May 2016

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Correction: Targeted Next-Generation Sequencing for Clinical Diagnosis of 561 Mendelian Diseases.
Yanqiu Liu, Xiaoming Wei, Xiangdong Kong, Xueqin Guo, Yan Sun, Lique Du

PLoS One· May 2016

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Correction: Targeted Next-Generation Sequencing for Clinical Diagnosis of 561 Mendelian Diseases.
Yanqiu Liu, Xiaoming Wei, Xiangdong Kong, Xueqin Guo, Yan Sun, Lique Du

PLoS One· December 2015

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