Association of insulin-like growth factor-1 polymorphisms with high myopia in the Chinese population

Benzer Materyaller

• A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family
  Yazar:: Sheng, Xunlun, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Targeted Next-generation Sequencing Reveals Novel EYS Mutations in Chinese Families with Autosomal Recessive Retinitis Pigmentosa
  Yazar:: Chen, Xue, ve diğerleri
  Baskı/Yayın Bilgisi: (2015)
• Association of IGF1 single-nucleotide polymorphisms with myopia in Chinese children
  Yazar:: Cheng, Tianyu, ve diğerleri
  Baskı/Yayın Bilgisi: (2020)
• Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia
  Yazar:: Sheng, Xunlun, ve diğerleri
  Baskı/Yayın Bilgisi: (2015)
• The association of lumican polymorphisms and high myopia in a Southern Chinese population
  Yazar:: Wang, Gui-Fang, ve diğerleri
  Baskı/Yayın Bilgisi: (2017)