Disruption of the Bipartite Imprinting Center in a Family with Angelman Syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference16 articles.
1. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting center on human chromosome 15;Buiting;Nat Genet,1995
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. 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
4. Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes;Buiting;Cytogenet Cell Genet,1999
5. Imprinting centre (IC) deletions in two PWS families: implications and strategies for diagnostic testing and genetic counselling;Buiting;Clin Genet,2000
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