SHOX point mutations and deletions in Leri-Weill dyschondrosteosis

Lignende værker

• Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male
  af: Stuppia, L, et al.
  Udgivet: (1999)
• Longitudinal Observation of a Patient with Leri-Weill Dyschondrosteosis and SHOX Haploinsufficiency
  af: Miyoshi, Yoko, et al.
  Udgivet: (2005)
• A Leri-Weill dyschondrosteosis patient confirmed by mutation analysis of SHOX gene
  af: Choi, Won Bok, et al.
  Udgivet: (2015)
• Characterization of SHOX Deletions in Léri-Weill Dyschondrosteosis (LWD) Reveals Genetic Heterogeneity and No Recombination Hotspots
  af: Benito-Sanz, Sara, et al.
  Udgivet: (2006)
• A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis
  af: Benito-Sanz, Sara, et al.
  Udgivet: (2005)