Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma

Lignende værker

• Mutation spectrum of PAX6 in Chinese patients with aniridia
  af: Zhang, Xiaohui, et al.
  Udgivet: (2011)
• A recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family
  af: Xiao, Xueshan, et al.
  Udgivet: (2011)
• Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy
  af: Chen, Yabin, et al.
  Udgivet: (2013)
• Mutational screening of six genes in Chinese patients with congenital cataract and microcornea
  af: Sun, Wenmin, et al.
  Udgivet: (2011)
• Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma
  af: Yang, Mei, et al.
  Udgivet: (2009)