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Craniosynostosis associated with partial duplication of 15q and deletion of 2q

โœ Scribed by Van Allen, M. I. ;Siegel-Bartelt, J. ;Feigenbaum, A. ;Teshima, I. E.


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
464 KB
Volume
43
Category
Article
ISSN
0148-7299

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We report an infant with multiple congenital anomalies, including craniosynostosis, tetralogy of Fallot variant, and limb anomalies associated with a maternal deletion of 15q15-22.1. Only two other patients have been reported with a similar deletion, but the deletion was paternal in both cases. We r