Q. Hou

发表

Experimental endometriosis reduction in rats treated with pioglitazone

Dongyun Zhang, M. He, Hong-yan Liu, 2012 .

Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population

Hong-yan Liu, Hongdan Wang, Xichuan Li, 2018, Scientific Reports.

[Analysis of CYP17A1 gene mutation in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency].

Bing M. Zhang, Shu-xian Cui, S. Liao, 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis

Jingbin Yan, Hongdan Wang, B. Zhu, 2017, Molecular medicine reports.

The use of cffDNA in fetal sex determination during the first trimester of pregnancy of female DMD carriers.

Dong Wu, S. Liao, Tao Li, 2012, Intractable & rare diseases research.

[Genetic and prenatal diagnosis for a haemophilia A family with two novel mutations of F8 gene].

B. Zhang, Hong-yan Liu, S. Liao, 2017, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Maternal cell contamination of prenatal samples and the potential effects on prenatal diagnosis results].

Zhao‐Yang Zhang, S. Liao, Tao Li, 2013, Zhonghua fu chan ke za zhi.

Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report.

Hongdan Wang, Tao Wang, Dong Wu, 2017, Molecular medicine reports.

Novel heterozygous mutations of the INSR gene in a familial case of Donohue syndrome.

Hong-yan Liu, Hongdan Wang, Xichuan Li, 2017, Clinica chimica acta; international journal of clinical chemistry.

DNA methylation study of fetus genome through a genome-wide analysis

M. He, Hongdan Wang, B. Zhu, 2014, BMC Medical Genomics.

[Association of polymorphisms of HLA-DRB1 gene with unexplained recurrent spontaneous abortion in ethnic Hans from Henan].

M. He, Dong Wu, S. Liao, 2014, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

Hongdan Wang, Dong Wu, S. Liao, 2016, Journal of Biomedical Science.

Mutations in the RS1 gene in a Chinese family with X-linked juvenile retinoschisis.

Dong Wu, S. Liao, Y. Chu, 2012, Intractable & rare diseases research.

Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis.

Dong Wu, S. Liao, Y. Chu, 2016, Taiwanese journal of obstetrics & gynecology.

A novel MIP mutation in familial congenital nuclear cataracts.

Hong-yan Liu, Hongdan Wang, Zhe Liu, 2016, European journal of medical genetics.

Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population

Hong-yan Liu, Hongdan Wang, Xichuan Li, 2018, Scientific Reports.

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

Hongdan Wang, Dong Wu, S. Liao, 2016, Journal of Biomedical Science.

Genetic polymorphisms of 20 short tandem repeat loci from the Han population in Henan, China

Hongdan Wang, B. Zhu, Dong Wu, 2014 .

Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome

Hongdan Wang, S. Liao, Shuya Yang, 2023, Frontiers in Genetics.