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Mosaic imprinting defect in a patient with an almost typical expression of the Prader–Willi syndrome

✍ Scribed by Wey, Eva; Bartholdi, Deborah; Riegel, Mariluce; Nazlican, Hülya; Horsthemke, Bernhard; Schinzel, Albert; Baumer, Alessandra


Book ID
110026142
Publisher
Nature Publishing Group
Year
2004
Tongue
English
Weight
127 KB
Volume
13
Category
Article
ISSN
1018-4813

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## Abstract Prader–Willi syndrome (PWS) is caused by loss of paternally expressed genes in the 15q11‐q13 region. To further characterize alterations in gene expression in this classical obesity syndrome we used whole genome microarrays to study a PWS mouse model resulting from a paternally derived