A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients

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Bibliographic Details
Published in:American Journal of Medical Genetics Part A 2007, Vol.143A (24), p.3302-3308
Main Authors: Erickson, Robert P., de Ståhl, Teresita Díaz, Bruder, Carl E.G., Dumanski, Jan P.
Format: Report
Language:English
Subjects:
chromosomal microarray
DiGeorge syndrome
Opitz GBBB
velocardiofacial syndrome
Online Access:Get full text
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.32025