Related references
Note: Only part of the references are listed.New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle
A. De Luca et al.
CLINICAL GENETICS (2011)
Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome
Julien Barc et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2011)
A copy number variation morbidity map of developmental delay
Gregory M. Cooper et al.
NATURE GENETICS (2011)
MutationTaster evaluates disease-causing potential of sequence alterations
Jana Marie Schwarz et al.
NATURE METHODS (2010)
Chromosome 8p23.1 Deletions as a Cause of Complex Congenital Heart Defects and Diaphragmatic Hernia
Margaret J. Wat et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)
Fog2 is critical for cardiac function and maintenance of coronary vasculature in the adult mouse heart
Bin Zhou et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot
Steven C. Greenway et al.
NATURE GENETICS (2009)
Double outlet right ventricle: aetiologies and associations
D. Obler et al.
JOURNAL OF MEDICAL GENETICS (2008)
Candidate genes for congenital diaphragmatic hernia from animal models:: sequencing of FOG2 and PDGFRα reveals rare variants in diaphragmatic hernia patients
S. B. Bleyl et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2007)
Disruption of friend of GATA 2 gene (FOG-2) by a de novo t(8;10) chromosomal translocation is associated with heart defects and gonadal dysgenesis
P. Finelli et al.
CLINICAL GENETICS (2007)
Biventricular repair in double outlet right ventricle: surgical results based on the STS-EACTS International Nomenclature classification
JH Artrip et al.
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY (2006)
Fog2 is required for normal diaphragm and lung development in mice and humans
KG Ackerman et al.
PLOS GENETICS (2005)
Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot
A Pizzuti et al.
HUMAN MUTATION (2003)
The incidence of congenital heart disease
JIE Hoffman et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2002)
A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding Fog-2
EC Svensson et al.
NATURE GENETICS (2000)
FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium
SG Tevosian et al.
CELL (2000)
Share Paper
