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

Hemoglobin E disease in North Indian population: A report of 11 cases

By Kishore Bimal   Khare Pratima   Gupta Rashmi Jain   Bisht Sonali   Majumdar Kaushik  

Hematology, Vol. 12, Iss. 4, 2007-08 ,pp. : 343-347

Maney Publishing

Access to resources Recommend Favorite

Short insertion in a hemoglobin chain: Hb Esch, an unstable 1 variant with duplication of the sequence Ala 65 -Leu-Thr-Asn 68

By Prehu C.   Groff P.   Kalmes G.   Golinska B.   Riou J.   Prome D.   Richelme-David S.   Kiger L.   Ducrocq R.   Wajcman H.  

Blood Cells, Molecules, and Diseases, Vol. 31, Iss. 2, 2003-09 ,pp. : 234-239

Elsevier

Access to resources Recommend Favorite

Performance analysis of newly developed point‐of‐care hemoglobinometer (TrueHb) against an automated hematology analyzer (Sysmex XT 1800i) in terms of precision in hemoglobin measurement

By  

International Journal Of Laboratory Hematology, Vol. 37, Iss. 4, 2015-08 ,pp. : 483-485

John Wiley & Sons Inc

Access to resources Recommend Favorite

Oxidative crosslinking, spectrin and membrane interactions of hemoglobin mixtures in HbEβ-thalassemia

By Chakrabarti Abhijit   Datta Poppy   Bhattacharya Dipankar   Basu Sumanta   Saha Sutapa  

Hematology, Vol. 13, Iss. 6, 2008-12 ,pp. : 361-368

Maney Publishing

Access to resources Recommend Favorite