| Literature DB >> 2705472 |
J T Mascarello1, J F Bastian, M C Jones.
Abstract
We describe a chromosome 22 deletion in a patient with the DiGeorge malformation sequence as manifested by an interrupted aortic arch, mild thymic hypoplasia, and minor craniofacial anomalies. Although others have reported DiGeorge sequence patients with deletions derived from unbalanced translocations involving the chromosome 22 long arm, the small interstitial deletion described here appears to be unusual for patients with this disorder.Entities:
Mesh:
Year: 1989 PMID: 2705472 DOI: 10.1002/ajmg.1320320124
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299