The genetical interpretation of haemoglobin H disease

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The genetical interpretation of haemoglobin H disease

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Athens University thalassemia expertise unit: evolution, structure, perspectives and patients' expectations.

Detection of human cytomegalovirus and epstein-barr-virus by the polymerase chain-reaction in patients with Beta-thalassemia.

Efficacy and tolerability of formoterol Turbuhaler in children.

Variations of ferritin levels over a period of 15 years as a compliance chelation index in thalassemic patients.

Reactogenicity of DTPa-HBV/Hib vaccine administered as a single injection vs DTPa-HBV and Hib vaccines administered simultaneously at separate sites, to infants at 2, 4 and 6 months of age.

Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA].

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Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

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The genetical interpretation of haemoglobin H disease

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