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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: papassotiriou i. Hemoglobin. 1999 Nov;23(4):325-37. doi: 10.3109/03630269909090748. Hemoglobin. 1999. PMID: 10569721
Tissue oxygenation in patients with hemoglobinopathy H.
Papassotiriou I, Kanavakis E, Stamoulakatou A, Kattamis C. Papassotiriou I, et al. Pediatr Hematol Oncol. 1997 Jul-Aug;14(4):323-34. doi: 10.3109/08880019709041592. Pediatr Hematol Oncol. 1997. PMID: 9211537
283 results