Increased Prevalence of Immunoglobulin A Deficiency in Patients with the Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

Christopher A. Smith; Deborah A. Driscoll; Beverly S. Emanuel; Donna M. McDonald-McGinn; Elaine H. Zackai; Kathleen E. Sullivan

doi:10.1128/CDLI.5.3.415-417.1998

DOI: 10.1128/CDLI.5.3.415-417.1998

Article Information

DOI

https://doi.org/10.1128/CDLI.5.3.415-417.1998

PubMed

9606003

Published By

American Society for Microbiology Journals

History

Received October 24, 1997
Returned for modification December 26, 1997
Accepted March 2, 1998
Published online May 1, 1998.

Author Information

Christopher A. Smith¹,
Deborah A. Driscoll²,
Beverly S. Emanuel³,
Donna M. McDonald-McGinn³,
Elaine H. Zackai³ and
Kathleen E. Sullivan¹ *

Division of Immunologic and Infectious Diseases¹ and
Division of Human Genetics and Molecular Biology,³ The Children’s Hospital of Philadelphia, and
Department of Obstetrics and Gynecology, The University of Pennsylvania School of Medicine,² Philadelphia, Pennsylvania

↵* Corresponding author. Mailing address: Division of Immunologic and Infectious Diseases, The Children’s Hospital of Philadelphia, 34th St. and Civic Center Blvd., Philadelphia, PA 19104. Phone: (215) 590-4685. Fax: (215) 590-3044. E-mail:sullivak{at}mail.med.upenn.edu.

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Increased Prevalence of Immunoglobulin A Deficiency in Patients with the Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

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