Am J Med Genet. 1996 Mar 29;62(3):274-5.

Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome.

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Department of Pediatrics, University of Virginia Health Sciences Center, Charlottesville 22908, USA.

Abstract

This report is on a 14-month-old boy with manifestations of Opitz (G/BBB) syndrome in whom a 22q11.2 deletion was found. Deletion analysis was requested because of some findings in this patient reminiscent of velocardiofacial (VCF) syndrome. The extent of aspiration and of respiratory symptoms in this child is not usually seen in VCF syndrome. Opitz syndrome maps to at least two loci, one on Xp, the other on 22q11.2.

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A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients. [Am J Med Genet A. 2007]
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Cited by 5 PubMed Central articles

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Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome.
Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome.
Am J Med Genet. 1996 Mar 29 ;62(3):274-5.

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