The first antenatal diagnosis of KBG syndrome: a microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD11 associated with the disorder

Lignende værker

• The first antenatal diagnosis of KBG syndrome: a microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD11 associated with the disorder
  af: Victoria Hodgetts Morton, et al.
  Udgivet: (2018-01-01)
• Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases
  af: Novara, Francesca, et al.
  Udgivet: (2017)
• Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome
  af: Willemsen, Marjolein H, et al.
  Udgivet: (2010)
• Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3
  af: Polvi, A., et al.
  Udgivet: (2012)
• A de novo Microdeletion of ANKRD11 Gene in a Korean Patient with KBG Syndrome
  af: Lim, Ji-Hun, et al.
  Udgivet: (2014)