β-Thalassemia Repository

This publication has 63 references indexed in Scilit:

• A new mutation at IVS1 nt 2(T----A), in beta-thalassemia from Algeria
  Blood, 1990
• A new codon 71 (+T) mutant resulting in beta zero thalassemia [letter]
  Blood, 1989
• A novel beta-thalassemia frameshift mutation (codon 14/15), detectable by direct visualization of abnormal restriction fragment in amplified genomic DNA
  Blood, 1988
• New amber mutation in a beta-thalassemic gene with nonmeasurable levels of mutant messenger RNA in vivo.
  Journal of Clinical Investigation, 1988
• Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114
  Blood, 1988
• A novelβthalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3′ end of IVS 2
  Nucleic Acids Research, 1988
• A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicing
  Blood, 1987
• Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family [published erratum appears in Blood 1986 Jul;68(1):323]
  Blood, 1986
• β-Thalassemia resulting from a single nucleotide substitution in an acceptor splice site
  Nucleic Acids Research, 1985
• beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.
  Proceedings of the National Academy of Sciences, 1984