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Cardiac anomalies in Axenfeld–Rieger syndrome due to a novel FOXC1 mutation |
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| Authors: | Karen W. Gripp M.D. Elizabeth Hopkins Kim Jenny Deepika Thacker Jonathan Salvin |
| Affiliation: | 1. Division of Medical Genetics, A. I. DuPont Hospital for Children, Wilmington, Delaware;2. Department of Cardiology, A. I. DuPont Hospital for Children, Wilmington, Delaware;3. Division of Ophthalmology, A. I. DuPont Hospital for Children, Wilmington, Delaware |
| Abstract: | |
| Keywords: | Axenfeld– Rieger syndrome ASD Congenital heart defect Hip dysplasia FOXC1 PITX2 |