Q. Cao

Short QT syndrome: a case report and review of literature.

Wei Zhou, Li-xiong Lu, Xingyu Zhang, 2006, Resuscitation.

Exome sequencing reveals a de novo PRKG1 mutation in a sporadic patient with aortic dissection

Wei Zhou, Wei Zhou, Q. Cao, 2018, BMC Medical Genetics.

Whole exome sequencing reveals a stop-gain mutation of PKD2 in an autosomal dominant polycystic kidney disease family complicated with aortic dissection

Wei Zhou, Q. Cao, Weimin Zhou, 2018, BMC Medical Genetics.

A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in Asians.

K. Hsiao, J. Reichardt, A. Ohtake, 2001, American journal of human genetics.

The Spectrum of ACAN Gene Mutations in a Selected Chinese Cohort of Short Stature: Genotype-Phenotype Correlation

Xiaonan Li, Wei Zhou, Zhanjun Jia, 2022, Frontiers in Genetics.

Exome sequencing identified a novel SMAD2 mutation in a Chinese family with early onset aortic aneurysms.

Q. Cao, Houqun Ying, Weimin Zhou, 2017, Clinica chimica acta; international journal of clinical chemistry.

Familial early-onset deep venous thrombosis associated with a novel HRG mutation.

Q. Cao, Weimin Zhou, Wei Zhou, 2017, European journal of medical genetics.

Short QT syndrome: a case report and review of literature.

Wei Zhou, Li-xiong Lu, Xingyu Zhang, 2006, Resuscitation.