Spatial and temporal silencing of the human maternal UBE3A gene

Author:

Daily Jennifer,Smith Amanda G.,Weeber Edwin J.

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference27 articles.

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3. Angelman syndrome;Clayton-Smith;Journal of Medical Genetics,1992

4. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance;Kaplan;American Journal of Medical Genetics,1987

5. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15;Buiting;Nature Genetics,1995

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