Yongchao Yang

发表

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.

Ankyrin repeat domain 1: A novel gene for cardiac septal defects

Jimei Chen, J. Zhuang, Xiaobing Liu, 2019, The journal of gene medicine.

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.

Pulmonary artery reconstruction and correction of tetralogy of Fallot combined with the absence of the mediastinal left pulmonary artery

Jimei Chen, J. Zhuang, J. Cen, 2022, Journal of cardiac surgery.

Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease

J. Zhuang, Yueheng Wu, Shufang Huang, 2018, Prenatal diagnosis.

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

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

Clinical application of chromosomal microarray analysis for the diagnosis of Williams–Beuren syndrome in Chinese Han patients

J. Zhuang, Yueheng Wu, Shufang Huang, 2018, Molecular genetics & genomic medicine.

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.

A novel GATA-binding protein 4 gene variation associated with familial atrial septal defect

Jimei Chen, J. Zhuang, Xiaobing Liu, 2018, bioRxiv.