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Phenotype of a patient with contiguous deletion of TBX5 and TBX3: Expanding the disease spectrum
Authors:Soujanya Bogarapu  Steven B. Bleyl  Amy Calhoun  David Viskochil  Elizabeth V. Saarel  Melanie D. Everitt  Deborah U. Frank
Affiliation:1. Division of Pediatric Cardiology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah;2. Division of Pediatric Genetics and Metabolism, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota;3. Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah;4. Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah
Abstract:
Keywords:TBX5  TBX3  Holt–  Oram syndrome  ulnar–  mammary syndrome  cardiac development  conduction system  congenital heart disease  arrhythmia
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