Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome
- PMID: 6854451
- DOI: 10.1016/s0022-3476(83)80014-6
Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome
Abstract
Two unrelated children with features of Beckwith-Wiedemann syndrome have been found to have partial duplication of chromosome 11p. A review of six other reported cases of partial duplication of 11 p revealed features of this syndrome not previously recognized. We suggest that karyotype studies with banding techniques should be done in children with features of Beckwith-Wiedemann syndrome and developmental delay or retardation.
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