Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference22 articles.
1. Disruption of the bipartite imprinting center in a family with Angelman syndrome;Buiting;Am J Hum Genet,2001
2. 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
3. Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counseling;Buiting;Clin Genet,2000
4. A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp;Buiting;Hum Genet,1999
5. 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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