Junction Site Analysis of Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency

Lignende værker

• Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
  af: Chen, Wuyan, et al.
  Udgivet: (2012)
• Comprehensive Genetic Analysis of 182 Unrelated Families with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
  af: Finkielstain, Gabriela P., et al.
  Udgivet: (2011)
• Comprehensive Mutation Analysis of the CYP21A2 Gene: An Efficient Multistep Approach to the Molecular Diagnosis of Congenital Adrenal Hyperplasia
  af: Xu, Zhi, et al.
  Udgivet: (2013)
• The Phenotypic Spectrum of Contiguous Deletion of CYP21A2 and Tenascin XB: Quadricuspid Aortic Valve and Other Midline Defects
  af: Chen, Wuyan, et al.
  Udgivet: (2009)
• Approach to the Adult with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
  af: Merke, Deborah P.
  Udgivet: (2008)