Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference28 articles.
1. Angelman syndrome due to uniparental disomy of chromosome 15: A milder phenotype?;Bottani;Am J Med Genet,1994
2. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15;Buiting;Nature Genet,1995
3. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome;Butler;Am J Med Genet,1986
4. Hypopigmentation: A common feature of the Prader-Labhart-Willi syndrome;Butler;Am J Hum Genet,1989
5. Prader-Willi syndrome;Cassidy;Curr Probl Pediatr,1984
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