Complete DiGeorge syndrome: Development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases

Author:

Louise Markert M,Alexieff Marilyn J,Li Jie,Sarzotti Marcella,Ozaki Daniel A,Devlin Blythe H,Sempowski Gregory D,Rhein Maria E,Szabolcs Paul,Hale Laura P,Buckley Rebecca H,Coyne Katharine E,Rice Henry E,Mahaffey Samuel M,Skinner Michael A

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference37 articles.

1. Embryologic and other developmental considerations of thirty-eight possible variants of the DiGeorge Anomaly (DGA);Thomas;Am J Med Genet,1987

2. A prospective cytogenetic study of 36 cases of DiGeorge syndrome;Wilson;Am J Hum Genet,1992

3. The spectrum of the DiGeorge syndrome;Conley;J Pediatr,1979

4. A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11;Driscoll;Am J Hum Genet,1992

5. The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge Syndrome;Van Esch;Genet Couns,1999

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