A case of Lenz microphthalmia syndrome.

Lignende værker

• A Rare Case of the Lenz Syndrome
  af: T, Sohil, et al.
  Udgivet: (2013)
• A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signaling pathway and causes Lenz microphthalmia syndrome
  af: Esmailpour, Taraneh, et al.
  Udgivet: (2014)
• BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects
  af: Hilton, Emma, et al.
  Udgivet: (2009)
• Conotruncal heart defect/microphthalmia syndrome: delineation of an autosomal recessive syndrome.
  af: Digilio, M C, et al.
  Udgivet: (1997)
• Association of a de novo 16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes
  af: Bardakjian, Tanya M, et al.
  Udgivet: (2009)