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Dergiler / Turkish Journal of Hematology / 2009 / Cilt: 26 - Sayı: 2

Compound heterozygosity for Hb D-Punjab / β-thalassemia and blood donation: Case report

Stamatia THEODORIDOU
Michael ALEMAYECHOU
Parthena PERPERIDOU
Clio SINOPOULOU
Theano KARAFOULIDOU
Georgia KIRIAKOPOULOU
Sayfa
100–101
DOI
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THEODORIDOU, S., ALEMAYECHOU, M., PERPERIDOU, P., SINOPOULOU, C., KARAFOULIDOU, T., KIRIAKOPOULOU, G. (2009). Compound heterozygosity for Hb D-Punjab / β-thalassemia and blood donation: Case report. Turkish Journal of Hematology, Cilt: 26 - Sayı: 2, 100–101. https://ajindex.com/articles/413382

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Kaynakça (5)

  1. Rahimi Z, Akramipour R, Korani S, Nagel RL. Hb D-Punjab [β 121(GH4) Glu-Gln]/βο-thalassemia [IVSII.1(G-A)] in two cases from an Iranian family: first report. Am J Hematol 2006;81:302-3
  2. Perea FJ, Casas-Castaneda M, Villalobos-Arambula AR, Barajas H, Alvarez F, Camacho A, Hermosillo RM, Ibarra B. Hb D-Los Angeles associated with Hb S or β-thalassemia in four Mexican Mestizo families. Hemoglobin 1999;23:231-7
  3. Adekile AD, Kazanetz EG, Leonova JY, Marouf R, Khmis A, Huisman TH. Co inheritance of Hb D-Punjab (codon 121:GAA-GAA and beta (0) thalassemia (IVSII 1;G-A). J Pediatr Hematol Oncol 1996;18:151-3
  4. Weatherall DJ, Glegg JB. The Thalassemia Syndromes. 4th ed. Oxford (UK): Blackwell Science, 2001
  5. Tsistrakis GA, Scampardonis GJ, Clonizakis JP, Concouris LL. Haemoglobin D and D thalassaemia. A family report, comprising 18 members. Acta Haematol 1975;54:172-9.