22q11.2 deletion syndrome and selective IgM deficiency: an association of a common chromosomal abnormality with a rare immunodeficiency

Am J Med Genet A. 2004 May 15;127A(1):99-100. doi: 10.1002/ajmg.a.20639.

Authors

Waleed Al-Herz¹, Stephen J McGeady¹, Karen W Gripp²

Affiliations

¹ Division of Allergy and Clinical Immunology, Nemours Children's Clinic, Wilmington, Alfred I. duPont Hospital for Children, Wilmington, Delaware, and Thomas Jefferson University, Philadelphia, Pennsylvania.
² Division of Medical Genetics, Nemours Children's Clinic, Wilmington, Alfred I. duPont Hospital for Children, Wilmington, Delaware, and Thomas Jefferson University, Philadelphia, Pennsylvania.

PMID: 15103727
DOI: 10.1002/ajmg.a.20639

No abstract available

Publication types

Letter

MeSH terms

Adolescent
Chromosome Deletion*
Chromosome Disorders / diagnosis*
Chromosome Disorders / genetics
Chromosomes, Human, Pair 22 / genetics*
Female
Humans
Immunoglobulin M / deficiency*
Immunologic Deficiency Syndromes / diagnosis*
Immunologic Deficiency Syndromes / genetics*

Substances

Immunoglobulin M