FGFR2 molecular analysis and related clinical findings in one Chinese family with Crouzon Syndrome

Lignende værker

• Ala344Pro mutation in the FGFR2 gene and related clinical findings in one Chinese family with Crouzon syndrome
  af: Lin, Ying, et al.
  Udgivet: (2012)
• Molecular analysis of FGFR 2 and associated clinical observations in two Chinese families with Crouzon syndrome
  af: Lin, Ying, et al.
  Udgivet: (2016)
• Molecular analysis of the choroideremia gene related clinical findings in two families with choroideremia
  af: Lin, Ying, et al.
  Udgivet: (2011)
• PAX6 analysis of one family and one sporadic patient from southern China with classic aniridia
  af: Lin, Ying, et al.
  Udgivet: (2011)
• FGFR2 mutation in a Chinese family with unusual Crouzon syndrome
  af: Li, Zi-Li, et al.
  Udgivet: (2016)