Novel Missense Variants of ZFPM2/FOG2 Identified in Conotruncal Heart Defect Patients Do Not Impair Interaction with GATA4

Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic tetralogy of fallot and double outlet right ventricle in a Chinese Han population

(2014) Xiaomin Huang et al.   MOLECULAR BIOLOGY REPORTS

Genetics of Congenital Heart Disease

(2013) Akl C. Fahed et al.   CIRCULATION RESEARCH

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

(2013) Charlotte Andreasen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

NovelZFPM2/FOG2variants in patients with double outlet right ventricle

(2011) Z-P Tan et al.   CLINICAL GENETICS

Performance of mutation pathogenicity prediction methods on missense variants

(2011) Janita Thusberg et al.   HUMAN MUTATION

Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion Syndrome

(2010) Kazuo Momma   AMERICAN JOURNAL OF CARDIOLOGY

New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle

(2010) A De Luca et al.   CLINICAL GENETICS

A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations

(2009) Chi Yang et al.   ELECTROPHORESIS

The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine

(2009) L. G. Biesecker et al.   GENOME RESEARCH

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

(2009) Steven C Greenway et al.   NATURE GENETICS

Functional and structural basis of the nuclear localization signal in the ZIC3 zinc finger domain

(2008) Minoru Hatayama et al.   HUMAN MOLECULAR GENETICS