O33: Concordance of long-read genome sequencing with methylation calling with clinical testing for individuals with Prader-Willi or Angelman Syndrome*

Eitemau Tebyg

• Prader–Willi Syndrome with Angelman Syndrome in the Offspring
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• P574: Molecular diagnosis of Prader-Willi and Angelman syndromes using methylation-specific MLPA
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