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

✍ Scribed by Mohammad Taghi Akbari; Mohammad Hamid; Mina Izadyar


Book ID
105989646
Publisher
Springer
Year
2010
Tongue
English
Weight
113 KB
Volume
90
Category
Article
ISSN
0939-5555

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