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Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha2, codon 59, GGC-->GAC) or a nondeletional alpha-thalassemia mutation (AATAAA-->AATAAG): comparison of phenotypes illustrating "dominant" alpha-thalassemia.
Traeger-Synodinos J, Metaxotou-Mavrommati A, Karagiorga M, Vrettou C, Papassotiriou I, Stamoulakatou A, Kanavakis E. Traeger-Synodinos J, et al. Among authors: kanavakis e. Hemoglobin. 1999 Nov;23(4):325-37. doi: 10.3109/03630269909090748. Hemoglobin. 1999. PMID: 10569721
Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes.
Maragoudaki E, Kanavakis E, Traeger-Synodinos J, Vrettou C, Tzetis M, Metaxotou-Mavrommati A, Kattamis C. Maragoudaki E, et al. Among authors: kanavakis e. Br J Haematol. 1999 Dec;107(4):699-706. doi: 10.1046/j.1365-2141.1999.01788.x. Br J Haematol. 1999. PMID: 10606872 Free article.
Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels.
Vrettou C, Kanavakis E, Traeger-Synodinos J, Metaxotou-Mavrommati A, Basiakos I, Maragoudaki E, Stamoulakatou A, Papassotiriou I, Kattamis C. Vrettou C, et al. Among authors: kanavakis e. Hemoglobin. 2000 Aug;24(3):203-20. doi: 10.3109/03630260008997528. Hemoglobin. 2000. PMID: 10975440
276 results