Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.

Gelijkaardige items

• Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobin.
  door: Stoeckert, C J, et al.
  Gepubliceerd in: (1987)
• Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China
  door: Zhang, Jie, et al.
  Gepubliceerd in: (2019)
• Deletion of a region that is a candidate for the difference between the deletion forms of hereditary persistence of fetal hemoglobin and deltabeta-thalassemia affects beta- but not gamma-globin gene expression.
  door: Calzolari, R, et al.
  Gepubliceerd in: (1999)
• High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin.
  door: Arcasoy, M O, et al.
  Gepubliceerd in: (1997)
• Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.
  door: Orkin, S H, et al.
  Gepubliceerd in: (1979)