Molecular Mechanism of Angelman Syndrome in Two Large Families Involves an Imprinting Mutation
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference42 articles.
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3. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint switch models, genetic counseling, and prenatal diagnosis;Buiting;Am J Hum Genet,1998
4. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting center on human chromosome 15;Buiting;Nat Genet,1995
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