Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)
<p>Abstract</p> <p>The Immunodeficiency, Centromeric region instability, Facial anomalies syndrome (ICF) is a rare autosomal recessive disease described in about 50 patients worldwide and characterized by immunodeficiency, although B cells are present, and by characteristic rearran...
| Published in: | Orphanet Journal of Rare Diseases |
|---|---|
| Main Authors: | , , |
| Format: | Article |
| Language: | English |
| Published: |
BMC
2006-03-01
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| Online Access: | http://www.OJRD.com/content/1/1/2 |
