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• Phenotypical and genotypical expansion of autosomal-dominant KDM1A-related neurodevelopmental disorder spectrum: a case report
  Article (Journal), Online Resource
• Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes
  Article (Journal), Online Resource

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Related Authors

• Schaaf, Christian P.
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