The Current Status of β-Thalassemia Major in Mainland China

By Xu Lu-Hong   Fang Jian-Pei  

Hemoglobin, Vol. 37, Iss. 4, 2013-08 ,pp. : 307-314

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The Changing Epidemiology of β-Thalassemia in the Greek-Cypriot Population

By Kyrri Andreani R.   Kalogerou Eleni   Loizidou Dena   Ioannou Christina   Makariou Christina   Kythreotis Loukas   Phylactides Marios   Kountouris Petros   Angastiniotis Michael   Modell Bernadette   Kleanthous Marina  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 435-443

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The Spectrum of β-Thalassemia Mutations in Baghdad, Central Iraq

By Al-Allawi Nasir A.S.   Al-Mousawi Bassam M.S.   Badi Ameer I.A.   Jalal Sana D.  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 444-453

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Utility Of The Multivariate Approach In Predicting β-Thalassemia Intermedia Or β-Thalassemia Major Types In Iranian Patients

By Banan Mehdi   Bayat Hadi   Namdar-Aligoodarzi Pegah   Azarkeivan Azita   Kamali Koorosh   Daneshmand Parvaneh   Zaker-Kandjani Behzad   Najmabadi Hossein  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 413-422

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Normal Hb A 2 β-Thalassemia Trait: Frameshift Mutation ( HBB : c.187_251dup) in Cis with the Hb A 2' δ-Globin Gene Missense Mutation ( HBD : c.49G>C)

By Waye John S.   Eng Barry   Hellens Laurie   Hohenadel Betty-Ann   Nakamura Lisa M.   Walker Lynda  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 201-204

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