Frequency of 22q11 deletions in patients with conotruncal defects. [electronic resource]
Producer: 19980901Description: 492-8 p. digitalISSN:- 0735-1097
- Aorta, Thoracic -- abnormalities
- Child
- Chromosome Deletion
- Chromosomes, Human, Pair 22 -- genetics
- DiGeorge Syndrome -- genetics
- Double Outlet Right Ventricle -- genetics
- Face -- abnormalities
- Female
- Genetic Testing
- Heart Defects, Congenital -- genetics
- Heart Septal Defects, Ventricular -- genetics
- Humans
- Incidence
- Male
- Prospective Studies
- Pulmonary Artery -- abnormalities
- Syndrome
- Tetralogy of Fallot -- genetics
- Transposition of Great Vessels -- genetics
- Truncus Arteriosus, Persistent -- genetics
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Publication Type: Comparative Study; Journal Article; Research Support, U.S. Gov't, P.H.S.
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