Familial Inheritance in Congenital Heart Disease: A Focus on Tetralogy of Fallot
Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart disease (CHD). The understanding of the genetics and inheritance of TOF is limited. Although about 15% of cases are associated with a 22q11.2 deletion, the majority have no known aetiology. Even in 22q11.2 Deletion Syndrome (22q1...
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| Language: | en_ca |
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2011
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| Online Access: | http://hdl.handle.net/1807/31423 |