Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference16 articles.
1. Di George syndrome and 22q11 rearrangements
2. Thymus deficiency in an infant with a chromosome t(18;22)(q12.2;p11.2)pat rearrangement
3. Spectrum of the DiGeorge “syndrome”
4. A deletion in chromosome 22 can cause digeorge syndrome
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3. Mosaic tetraploidy in a liveborn infant with features of the DiGeorge anomaly;Clinical Genetics;2008-06-28
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