Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder

Similar Items

• A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles
  od: Abu-Amero, Khaled K., i dr.
  Izdano: (2017)
• A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles
  od: Khaled K. Abu-Amero, i dr.
  Izdano: (2017-11-01)
• Recent Progress in Understanding Congenital Cranial Dysinnervation Disorders
  od: Oystreck, Darren T., i dr.
  Izdano: (2011)
• A congenital cranial dysinnervation disorder: Möbius’ syndrome
  od: Albayrak, Hatice Mutlu, i dr.
  Izdano: (2017)
• Congenital third cranial nerve palsy with prenuclear dysinnervation involving otolithic pathways: Underpinnings of a novel congenital cranial dysinnervation disorder
  od: Pandey, Pramod K, i dr.
  Izdano: (2020)