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Title: Deletion of chromosome 11(p11p13) in a patient with Beckwith-Wiedemann syndrome. Author: Schmutz SM. Journal: Clin Genet; 1986 Sep; 30(3):154-6. PubMed ID: 3780031. Abstract: Four cases of duplication of a segment of 11p have been reported in patients with Beckwith-Wiedemann syndrome (Waziri et al. 1983, Turleau et al. 1984). We describe a patient with Beckwith-Wiedemann syndrome who has a deletion of chromosome 11(p11p13) and suggest involvement of this chromosomal region in both the duplicated and deleted states such as occurs in Prader-Willi syndrome.[Abstract] [Full Text] [Related] [New Search]