Phenotypes of autism spectrum disorder and schizoaffective disorder associated with SETD1B gene but without intellectual disability and seizures

Ejemplares similares

• Cohen syndrome: Can early‐onset recurrent infections and hypotonia provide early diagnosis and intervention for intellectual disability?
  por: Gül Ünsel‐Bolat, et al.
  Publicado: (2024)
• A novel MAOA gene variant: Brunner syndrome, a rare syndrome, is associated with a wide range of psychiatric symptoms
  por: Gül Ünsel‐Bolat, et al.
  Publicado: (2024)
• Investigation of patients with childhood epilepsy in single center: Comprehensive genetic testing experience
  por: Hamide Betul Gerik‐Celebi, et al.
  Publicado: (2024)
• Clinical Insights Into a Rare SETD2 Disorder: Report of a Novel Variant
  por: Gül Ünsel‐Bolat, et al.
  Publicado: (2025)
• Testing DAT1 and DRD4 Genes in Attention Deficit Hyperactivity Disorder Using a Wide Spectrum of Neurocognitive Batteries
  por: Gül Ünsel‐Bolat, et al.
  Publicado: (2026)