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Article

Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family.

Annals of hematology - 1 Mar 2011

Akbari Mohammad Taghi, Hamid Mohammad, Izadyar Mina

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Share to Anemia, Hemolytic
Share to beta-Thalassemia
Share to Blood Transfusion
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Hemoglobins, Abnormal

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Identifiers

PMID: 20521148
DOI: 10.1007/s00277-010-1003-4

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Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family.PMID 20521148Read ↗

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