Weizhi Zhang

发表

A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region.

Li Xie, Jian Wang, Yi-feng Yang, 2013, Gene.

Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome

B. Yin, Cheng Luo, Jian Wang, 2012, American journal of medical genetics. Part A.

Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death

Li Xie, Jian Wang, Yi-feng Yang, 2014, Scientific Reports.

Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome

Xiaohui Xie, Yi-qiao Hu, Yi-feng Yang, 2021, Frontiers in Cardiovascular Medicine.

Correction: Whole-exome sequencing identifies a novel CCDC151 mutation, c.325GT (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus

Zhiping Tan, T. Guo, Hong Luo, 2019, Journal of Human Genetics.

Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus

Zhiping Tan, T. Guo, Hong Luo, 2018, Journal of Human Genetics.

Rare De Novo Copy Number Variants in Patients with Congenital Pulmonary Atresia

T. Zhao, Li Xie, Jian Wang, 2014, PloS one.

1q21.1 microduplication in a patient with mental impairment and congenital heart defect

Zhiping Tan, L. Fan, Yifeng Yang, 2015, Molecular medicine reports.

Duplication of 10q22.3–q23.3 encompassing BMPR1A and NGR3 associated with congenital heart disease, microcephaly, and mild intellectual disability

T. Zhao, Li Xie, Jian Wang, 2015, American journal of medical genetics. Part A.

Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly.

Hong Luo, Li Xie, Jian Wang, 2012, European journal of medical genetics.