Interaction of Hb Adana ( HBA2 : c.179G>A) with Deletional and Nondeletional α + -Thalassemia Mutations: Diverse Hematological and Clinical Features

By Nainggolan Ita M.  

Hemoglobin, Vol. 37, Iss. 3, 2013-06 ,pp. : 297-305

Informa Healthcare

Access to resources Recommend Favorite

Hb Fulton-Georgia [α20(B1)His→Pro; HBA1: c.62A>C]: A New α-Globin Variant Coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC Disease

By Zhuang Lina   Patel Niren   Bryant Shanequa   Kutlar Abdullah   Kutlar Ferdane   Young Andrew N.  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 481-485

Informa Healthcare

Access to resources Recommend Favorite

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

Informa Healthcare

Access to resources Recommend Favorite

A Case of Alpha-Thalassemia-2 Associated with Pulmonary Infarction

By Hayashi Seiji   Matsuoka Hiroto   Harano Teruo   Harano Keiko   Nakahara Hiroshi   Tachibana Isao   Kida Hiroshi   Kawasaki Tomio   Kyotani Shingo   Oka Yoshihiro   Sakatani Mitsunori   Kawase Ichiro  

Lung, Vol. 184, Iss. 4, 2006-08 ,pp. : 223-227

Springer Publishing Company

Access to resources Recommend Favorite

Codon 62 (G T G>G C G, Val→Ala) ( α 1) ( HBA1 : c.188T>C) Causing Nondeletional α -Thalassemia in a Chinese Family

By Liao Can   Tang Hai-Shen   Li Ru   Li Dong-Zhi  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 188-191

Informa Healthcare

Access to resources Recommend Favorite