Related content

Complex interaction of Hb Q-Thailand and Hb E with α-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family

By Zheng Weidong   Liu Yanhui   Chen Dong   Rong Kabin   Ge Yanfen   Gong Caiping   Chen Heping  

Annals of Hematology, Vol. 89, Iss. 9, 2010-09 ,pp. : 883-888

Springer Publishing Company

Access to resources Recommend Favorite

Screening for co-existence of α-thalassemia in β-thalassemia and in HbE heterozygotes via an enzyme-linked immunosorbent assay for Hb Bart's and embryonic ζ-globin chain

By Tatu Thanusak  

International Journal of Hematology, Vol. 95, Iss. 4, 2012-04 ,pp. : 386-393

Springer Publishing Company

Access to resources Recommend Favorite

Identification of β thalassemia mutations in South Brazilians

By Reichert Vivian   Castro Simone   Wagner Sandrine   Albuquerque Dulcinéia   Hutz Mara   Leistner-Segal Sandra  

Annals of Hematology, Vol. 87, Iss. 5, 2008-05 ,pp. : 381-384

Springer Publishing Company

Access to resources Recommend Favorite

Neonatal screening for α‐thalassemia by cord hemoglobin Barts: how effective is it?

By  

International Journal Of Laboratory Hematology, Vol. 37, Iss. 5, 2015-10 ,pp. : 649-653

John Wiley & Sons Inc

Access to resources Recommend Favorite

Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease

By Sripichai Orapan   Munkongdee Thongperm   Kumkhaek Chutima   Svasti Saovaros   Winichagoon Pranee   Fucharoen Suthat  

Annals of Hematology, Vol. 87, Iss. 5, 2008-05 ,pp. : 375-379

Springer Publishing Company

Access to resources Recommend Favorite