Yonghua Wang

Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defects

Shaobin Lin, Yi Zhou, X. Ou, 2021, Molecular cytogenetics.

Screening and identification of potential predictive biomarkers for Down’s syndrome from second trimester maternal serum

B. Zhang, Yang Luo, Yuan Yao, 2015, Expert review of proteomics.

Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein-Taybi syndrome

H. Hakonarson, H. Qu, L. Tian, 2019, Orphanet Journal of Rare Diseases.

A Novel Mutation in MYH6 in Two Unrelated Chinese Han Families with Familial Atrial Septal Defect.

J. Zhuang, Yueheng Wu, Shufang Huang, 2019, Circulation. Genomic and precision medicine.

FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy

H. Hakonarson, H. Qu, Y. Liu, 2020, medRxiv.

Novel insertion mutation (Arg1822_Glu1823dup) in MYH6 coiled-coil domain causing familial atrial septal defect.

J. Zhuang, Yueheng Wu, Shufang Huang, 2021, European journal of medical genetics.

Prenatal diagnosis of Treacher Collins syndrome: A case report and literature review

Yanying Liu, Yonghua Wang, Yin Wang, 2023, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities

J. Zhuang, Yueheng Wu, Shufang Huang, 2019, Fetal and Pediatric Pathology.