Characterization of a New α-Thalassemia-1 Mutation in a Spanish Family

This publication has 15 references indexed in Scilit:

• A new gene deletion involving the α2‐, α1 ‐, and 81‐globin genes in a black family with Hb H disease
  American Journal of Hematology, 1992
• Identification of an extensive ζ‐α globin gene deletion in a Chinese individual
  British Journal of Haematology, 1992
• α-Globin Genotypes in a Spanish Population
  Hemoglobin, 1992
• A review of the molecular genetics of the human alpha-globin gene cluster
  Blood, 1989
• Characterization of a New α-Thalassemia-1 Deletion in a Spanish Family
  Hemoglobin, 1989
• Characterization of a newly discovered α‐thalassaemia‐1 in two Spanish patients with Hb H disease
  British Journal of Haematology, 1988
• Characterization of two deletions that remove the entire human ζ‐α globin gene complex (—^THAI and —^FIL)
  British Journal of Haematology, 1988
• Characterisation of a new α thalassemia 1 defect due to a partial deletion of the α globin gene complex
  Nucleic Acids Research, 1980
• Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.
  Proceedings of the National Academy of Sciences, 1980
• The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletions
  Cell, 1980