| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3193279 | Annals of Allergy, Asthma & Immunology | 2007 | 6 Pages |
Abstract
Fluorescence in situ hybridization analysis for chromosome 22q11.2 deletion should be considered in patients with selective IgM deficiency, especially if concurrent chronic otitis media, developmental delay, velopharyngeal insufficiency, or dysmorphic features are present.
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Authors
Shiang-Ju MD, Karen W. MD, Mark J. MD, Mary P. MD, Stephen J. MD,