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Autori: Chassanidis Christos

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Naslov Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the A gamma-158 C > T mutation in gamma-globin gene transcription (Letter)
Autori Kollia Panagoula Kalamaras Angelos Chassanidis Christos Samara Maria Vamvakopoulos Nikolaos K Radmilovic Milena M Pavlovic Sonja T Papadakis Manoussos N Patrinos George P 
Info BLOOD CELLS MOLECULES AND DISEASES, (2008), vol. 41 br. 3, str. 263-264
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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