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.

مواد مشابهة

• Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobin.
  بواسطة: Stoeckert, C J, وآخرون
  منشور في: (1987)
• Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China
  بواسطة: Zhang, Jie, وآخرون
  منشور في: (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.
  بواسطة: Calzolari, R, وآخرون
  منشور في: (1999)
• High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin.
  بواسطة: Arcasoy, M O, وآخرون
  منشور في: (1997)
• Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.
  بواسطة: Orkin, S H, وآخرون
  منشور في: (1979)