Mutations in the EGF-CFC Gene Cryptic Are an Infrequent Cause of Congenital Heart Disease

Congenital Heart Disease Caused by Mutations in the Transcription Factor <i>NKX2-5</i>

Jean‐Jacques Schott, D. Woodrow Benson, Craig T. Basson et al. · Science · 1998 · 1.3K citations

Life Sciences, Genetics, Molecular Genetics +17

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

Vidu Garg, Irfan S. Kathiriya, R. Bowling Barnes et al. · Nature · 2003 · 1.2K citations

Medicine, Genetics, Molecular Genetics +14

Different <i>TBX5</i> interactions in heart and limb defined by Holt–Oram syndrome mutations

Craig T. Basson, Taosheng Huang, Robert C. Lin et al. · Proceedings of the National Academy of Sciences · 1999 · 365 citations

Life Sciences, Genetics, Molecular Genetics +17

The <i>one-eyed pinhead</i> gene functions in mesoderm and endoderm formation in zebrafish and interacts with <i>no tail</i>

Alexander F. Schier, Stephan C. F. Neuhauss, Kathryn Ann Helde et al. · Development · 1997 · 360 citations

Life Sciences, Biology, Genetics +15

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

Richard N. Bamford, Erich Roessler, Rebecca D. Burdine et al. · Nature Genetics · 2000 · 351 citations

Life Sciences, Genetics, Molecular Genetics +12