Qinghua Zhou

发表

A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings

J. Mcgrath, H. Chai, A. Diadamo, 2019, Front. Genet..

Non-Invasive Prenatal Diagnosis: A Comparison of Cell Free Fetal DNA (cffDNA) Based Screening and Fetal Nucleated Red Blood Cell (fnRBC) Initiated Testing

Xinghua Pan, Qinghua Zhou, Peining Li, 2013 .

De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome

Qinghua Zhou, Peining Li, Jiansheng Xie, 2017, Molecular Cytogenetics.

A Cell‐free DNA Barcode‐Enabled Single‐Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β‐Thalassemia

Yuanping Du, Zhuo Song, Wanjun Zhou, 2019, Advanced science.

Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature

Weiqin Wu, Qinghua Zhou, Peining Li, 2015, Molecular Cytogenetics.

Bioinformatic and functional analysis of promoter region of human SLC25A13 gene.

Jing Chen, Qinghua Zhou, Zhanpeng Zhang, 2019, Gene.

Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature

Weiqin Wu, Qinghua Zhou, Peining Li, 2015, Molecular Cytogenetics.

Spectrum of Cytogenomic Abnormalities Revealed by Array Comparative Genomic Hybridization on Products of Conception Culture Failure and Normal Karyotype Samples.

Peining Li, A. Diadamo, Qinghua Zhou, 2016, Journal of genetics and genomics = Yi chuan xue bao.

Whole-exome sequencing analysis on products of conception: A cohort study to evaluate clinical utility and genetic etiology for pregnancy loss

U. Reddy, W. Mak, Qinghua Zhou, 2020, medRxiv.

A Pilot Study of Next-Generation Sequencing on Cell-Free DNA from Blood Plasma and Bone Marrow Fluid for Detecting Leukemic Clonal Abnormalities

Zongzhi Liu, Zongzhi Z. Liu, Qinghua Zhou, 2014 .

Novel homozygous FANCL mutation and somatic heterozygous SETBP1 mutation in a Chinese girl with Fanconi Anemia.

Weiqin Wu, Qinghua Zhou, Peining Li, 2017, European journal of medical genetics.

De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome

Qinghua Zhou, Peining Li, Jiansheng Xie, 2017, Molecular Cytogenetics.

Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses

Qinghua Zhou, J. Wen, Peining Li, 2023, Molecular genetics & genomic medicine.