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Prader-Willi syndrome: Consideration of a question in its clinical, cytogenetic and molecular aspects

✍ Scribed by Norio Niikawa


Publisher
Nature Publishing Group
Year
1990
Tongue
English
Weight
83 KB
Volume
35
Category
Article
ISSN
1435-232X

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Recent studies have identified a new class of Prader-Willi syndrome (PWS) and Angelman syndrome (AS) patients who have biparental inheritance, but neither the typical deletion nor uniparental disomy (UPD) or translocation. However, these patients have uniparental DNA methylation throughout 15q11-q13

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