Different Mechanisms and Recurrence Risks of Imprinting Defects in Angelman Syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference34 articles.
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2. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15;Buiting;Nat Genet,1995
3. Phenotypic differences in Angelman syndrome patients: imprinting mutations show less frequently microcephaly and hypopigmentation than deletions;Bürger;Am J Med Genet,1996
4. Interchromosomal transfer of epigenetic states in ascobolus: transfer of DNA methylation is mechanistically related to homologous recombination;Colot;Cell,1996
5. Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region;Dittrich;Hum Mol Genet,1993
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