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  • Ahmet Okay Çağlayan, Jacob F. Baranoski, +23 authors Murat Gunel
  • Medicine
  • Pediatric neurology
  • 2014 (First Publication: 1 December 2014)
  • BACKGROUND Knobloch syndrome is a rare, autosomal recessive, developmental disorder characterized by stereotyped ocular abnormalities with or without occipital skull deformities (encephalocele, boneContinue Reading