Frequency of 22q11 deletions in patients with conotruncal defects.
Goldmuntz, E
Frequency of 22q11 deletions in patients with conotruncal defects. [electronic resource] - Journal of the American College of Cardiology Aug 1998 - 492-8 p. digital
Publication Type: Comparative Study; Journal Article; Research Support, U.S. Gov't, P.H.S.
0735-1097
10.1016/s0735-1097(98)00259-9 doi
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
Frequency of 22q11 deletions in patients with conotruncal defects. [electronic resource] - Journal of the American College of Cardiology Aug 1998 - 492-8 p. digital
Publication Type: Comparative Study; Journal Article; Research Support, U.S. Gov't, P.H.S.
0735-1097
10.1016/s0735-1097(98)00259-9 doi
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