Detection of Hb Constant Spring [ α 142, Term→Gln, T AA> C AA ( α 2)] in Heterozygotes Combined With β-Thalassemia

By Li You-Qiong  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 197-200

Informa Healthcare

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Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A T Indian (AATA AA >AATA- -) Mutation in Four Indian Families

By Nair Sona B.   Nadkarni Anita H.   Ghosh Kanjaksha   Colah Roshan B.  

Hemoglobin, Vol. 37, Iss. 3, 2013-06 ,pp. : 277-284

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The Clinical and Laboratory Spectrum of Hb C [β6(A3)Glu→Lys, G AG> A AG] Disease

By Cook Cathleen M.  

Hemoglobin, Vol. 37, Iss. 1, 2013-02 ,pp. : 16-25

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A case of AA amyloidosis associated with rheumatoid arthritis effectively treated with Infliximab

By Kuroda Takeshi  

Rheumatology International, Vol. 28, Iss. 11, 2008-09 ,pp. : 1155-1159

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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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