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

Hb Papanui [α99(G8)Lys→Arg; HBA2: c.299A>G]: A Novel Silent Substitution Interfering in Hb A_1c Determination

By Brennan Stephen O.   Chan Tim  

Hemoglobin, Vol. 37, Iss. 6, 2013-12 ,pp. : 589-592

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

Commentary: Diagnostic Validity and Clinical Utility of HbA1c Tests for Type 2 Diabetes Mellitus

By  

Current Diabetes Reviews, Vol. 14, Iss. 2, 2018-03 ,pp. : 196-199

Bentham Science Publishers

Access to resources Recommend Favorite

Association of Hb Thailand [ α 56(E5)Lys→Thr] and Hb Phnom Penh [ α 117(GH5)-Ile- α 118(H1)] with α 0 -Thalassemia: Molecular and Hematological Features and Differential Diagnosis

By Singha Kritsada  

Hemoglobin, Vol. 37, Iss. 1, 2013-02 ,pp. : 37-47

Informa Healthcare

Access to resources Recommend Favorite