Report of a patient and further clinical and molecular characterization of interstitial 4p16.3 microduplication

समान संसाधन

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  प्रकाशित: (2015)
• A Private 16q24.2q24.3 Microduplication in a Boy with Intellectual Disability, Speech Delay and Mild Dysmorphic Features
  द्वारा: Palumbo, Orazio, और अन्य
  प्रकाशित: (2020)
• Whole Exome Sequencing Reveals a Novel AUTS2 In-Frame Deletion in a Boy with Global Developmental Delay, Absent Speech, Dysmorphic Features, and Cerebral Anomalies
  द्वारा: Palumbo, Pietro, और अन्य
  प्रकाशित: (2021)