Related references
Note: Only part of the references are listed.GATA4 mutations in 486 Chinese patients with congenital heart disease
Weimin Zhang et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2008)
We need a detailed phenome in the phenomenon of genetics and congenital heart disease
M. G. Posch et al.
JOURNAL OF MEDICAL GENETICS (2008)
Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects
Maximilian G. Posch et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
GATA4 sequence variants in patients with congenital heart disease
A. Tomita-Mitchell et al.
JOURNAL OF MEDICAL GENETICS (2007)
Spectrum of heart disease associated with murine and human GATA4 mutation
Satish K. Rajagopal et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2007)
Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease
Marie K. Schluterman et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Cardiac transcription factor Csx/Nkx2-5: its role in cardiac development and diseases
H Akazawa et al.
PHARMACOLOGY & THERAPEUTICS (2005)
Phenotypes with GATA4 or NKX2.5 mutations in familial artrial septal defect
K Hirayama-Yamada et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors
A Sarkozy et al.
JOURNAL OF MEDICAL GENETICS (2005)
A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family -: art. no. e97
A Okubo et al.
JOURNAL OF MEDICAL GENETICS (2004)
Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations
SM Reamon-Buettner et al.
AMERICAN JOURNAL OF PATHOLOGY (2004)
NKX2.5 mutations in patients with congenital heart disease
DB McElhinney et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2003)
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
V Garg et al.
NATURE (2003)
Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD
Y Watanabe et al.
JOURNAL OF MEDICAL GENETICS (2002)
The incidence of congenital heart disease
JIE Hoffman et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2002)
Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease
Y Ikeda et al.
CIRCULATION JOURNAL (2002)
NKX2.5 mutations in patients with tetralogy of Fallot
E Goldmuntz et al.
CIRCULATION (2001)
Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease
WD Zhu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Share Paper
