Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2003.00049.x/fullpdf
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4. DiGeorge syndrome: part of CATCH 22;Wilson;J Med Genet,1993
5. Velo-cardio-facial syndrome: a review of 120 patients;Goldberg;Am J Med Genet,1993
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