Related references
Note: Only part of the references are listed.Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations
Javier T. Granados-Riveron et al.
CONGENITAL HEART DISEASE (2012)
Congenital Heart Disease-Causing Gata4 Mutation Displays Functional Deficits In Vivo
Chaitali Misra et al.
PLOS GENETICS (2012)
The molecular genetics of congenital heart disease: a review of recent developments
Michael Wolf et al.
CURRENT OPINION IN CARDIOLOGY (2010)
An endocardial pathway involving Tbx5, Gata4, and Nos3 required for atrial septum formation
Mathieu Nadeau et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Molecular mechanisms of congenital heart disease
Huang Jing-bin et al.
CARDIOVASCULAR PATHOLOGY (2009)
Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development
Meenakshi Maitra et al.
DEVELOPMENTAL BIOLOGY (2009)
A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation
Alex V. Postma et al.
CIRCULATION RESEARCH (2008)
The developmental genetics of congenital heart disease
Benoit G. Bruneau
NATURE (2008)
Genetic basis for congenital heart defects: Current knowledge - A scientific statement from the American heart association congenital cardiac defects committee, council on cardiovascular disease in the young
Mary Ella Pierpont et al.
CIRCULATION (2007)
TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome
DA McDermott et al.
PEDIATRIC RESEARCH (2005)
SALL4 mutations Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders
J Kohlhase et al.
HUMAN MUTATION (2005)
Cardiac transcription factor Csx/Nkx2-5: its role in cardiac development and diseases
H Akazawa et al.
PHARMACOLOGY & THERAPEUTICS (2005)
Genetics of cardiological disorders
N Manning et al.
SEMINARS IN FETAL & NEONATAL MEDICINE (2005)
New insight into heart-hand'' syndromes: a newly discovered chromosomal abnormality in a family with heart-hand'' syndrome
S Adamopoulos et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2004)
Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy
J Kohlhase et al.
JOURNAL OF MEDICAL GENETICS (2003)
Functional analysis of TBX5 missense mutations associated with holt-oram syndrome
C Fan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Current advances in Holt-Oram syndrome
T Huang
CURRENT OPINION IN PEDIATRICS (2002)
Cardiac malformations associated with the Holt-Oram syndrome - Report on a family and review of the literature
T Bossert et al.
THORACIC AND CARDIOVASCULAR SURGEON (2002)
The incidence of congenital heart disease
JIE Hoffman et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2002)
A genetic blueprint for cardiac development
D Srivastava et al.
NATURE (2000)
Share Paper
