DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.

Author:

Wilson D I,Cross I E,Goodship J A,Coulthard S,Carey A H,Scambler P J,Bain H H,Hunter A S,Carter P E,Burn J

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

Reference25 articles.

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2. Congenital cardiovascular disease and anomalies of the third and fourth pharyngeal pouch;Freedom, R.M.; Rosen, F.S.; Nadas, A.S.;Circulation,1972

3. DiGeorge syndrome presenting as severe congenital heart disease in the newborn;Finley, J.P.; Collins, G.F.; De Chadarevian, J.P.; Williams, R.L.;Can Med Assoc J,1977

4. The spectrum of the DiGeorge syndrome;Conley, M.E.; Beckwith, J.B.; Mancer, J.F.K.; Tenckhoff, L.;J Pediatr,1979

5. Cardiovascular malformations in DiGeorge syndrome (congenital absence or hypoplasia of the thymus);Moerman, P.; Goddeeris, P.; Lauwerijns, J.; Van Der Hauwaert, L.G.;Br Heart J,1980

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