Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival

Author:

Winter W. E.,Silverstein J. H.,Barrett D. J.,Kiel E.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference13 articles.

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2. Barr DGD, Prader A, Esper U, Rampini S, Marvian VJ, Forfar JO (1971) Chronic hypoparathyroidism in two generations. helv Paediatr Acta 26:507?521

3. de la Chapelle A, Herva R, Koivisto M, Aula P (1981) A deletion in chromosome 22 can cause DiGeorge syndrome. Hum Genet 57:253?256

4. Freedom RM, Rosen FS, Nadas AS (1972) Congenital cardiovascular disease and anomalies of the third and fourth pharyngeal pouch. Circulation 46:165?172

5. Giles D, Iteld BJ, Rives KL (1981) The cardiomyopathy of hypoparathyroidism: Another reversible form of heart muscle disease. Chest 79:225?229

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1. Hypocalcemic tetany as an early sign of DiGeorge syndrome in an adult woman;The American Journal of Medicine;2002-02

2. Phenotype of adults with the 22q11 deletion syndrome: A review;American Journal of Medical Genetics;1999-10-08

3. Neonatal Calcium and Phosphorus Metabolism;Principles of Perinatal—Neonatal Metabolism;1998

4. Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome;American Journal of Medical Genetics;1997-03-03

5. Neonatal Mineral Metabolism;Principles of Perinatal-Neonatal Metabolism;1991

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