Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.

Author:

Robinson W P,Wagstaff J,Bernasconi F,Baccichetti C,Artifoni L,Franzoni E,Suslak L,Shih L Y,Aviv H,Schinzel A A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion;Knoll, J.H.M.; Nicholls, R.D.; Magenis, R.E.; JM, Jr, Graham; Lalande, M.; Latt, S.A.;Am J Med Genet,1989

2. Uniparental disomy in the Angelman syndrome;Malcolm, S.; Clayton-Smith, J.; Nichols, M.;Lancet,1991

3. Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome;Nicholls, R.D.; Pai, G.S.; Gottlieb, W.; Cantu, E.S.;Ann Neurol,1992

4. Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome;Nicholls, R.D.; Knoll, J.H.M.; Butler, M.G.; Karam, S.; LaLande, M.;Nature,1989

5. and clinical investigations of Prader-Willi syndrome patients;Robinson, W.P.; Bottani, A.; Yagang, X.;Am J Hum Genet,1991

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