Reciprocal Deletion and Duplication of 17p11.2-11.2: Korean Patients with Smith-Magenis Syndrome and Potocki-Lupski Syndrome

Lignende værker

• Neurodevelopmental Disorders Associated with Abnormal Gene Dosage: Smith–Magenis and Potocki–Lupski Syndromes
  af: Neira-Fresneda, Juanita, et al.
  Udgivet: (2015)
• 17p11.2 and Xq28 duplication detected in a girl diagnosed with Potocki–Lupski syndrome
  af: Sumathipala, Dulika S., et al.
  Udgivet: (2015)
• Opposing phenotypes in mice with Smith-Magenis deletion and Potocki -Lupski duplication syndromes suggest gene dosage effects on fluid consumption behavior
  af: Heck, Detlef H., et al.
  Udgivet: (2012)
• Phenotypic Consequences of Copy Number Variation: Insights from Smith-Magenis and Potocki-Lupski Syndrome Mouse Models
  af: Ricard, Guénola, et al.
  Udgivet: (2010)
• Mouse Models of Genomic Syndromes as Tools for Understanding the Basis of Complex Traits: An Example with the Smith-Magenis and the Potocki-Lupski Syndromes
  af: Carmona-Mora, P, et al.
  Udgivet: (2009)