Red cell membrane protein deficiencies in Mexican patients with hereditary spherocytosis

By Sanchez-Lopez J.Y.   Camacho A.L.   Magana M.T.   Ibarra B.   Perea F.J.  

Blood Cells, Molecules, and Diseases, Vol. 31, Iss. 3, 2003-11 ,pp. : 357-359

Elsevier

Access to resources Recommend Favorite

Ankyrin gene mutations in japanese patients with hereditary spherocytosis

By Nakanishi Hidekazu   Kanzaki Akio   Yawata Ayumi   Yamada Osamu   Yawata Yoshihito  

International Journal of Hematology, Vol. 73, Iss. 1, 2001-01 ,pp. : 54-63

Springer Publishing Company

Access to resources Recommend Favorite

Hematologically Important Mutations: Band 3 and Protein 4.2 Variants in Hereditary Spherocytosis

By Gallagher P.G.   Forget B.G.  

Blood Cells, Molecules, and Diseases, Vol. 23, Iss. 3, 1997-12 ,pp. : 417-421

Academic Press

Access to resources Recommend Favorite

Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders

By  

International Journal Of Laboratory Hematology, Vol. 40, Iss. 1, 2018-02 ,pp. : 94-102

John Wiley & Sons Inc

Access to resources Recommend Favorite

Hereditary spherocytosis: identification of several HS families with ankyrin and band 3 deficiency in a population of southwestern Poland

By Bogusławska D.  

Annals of Hematology, Vol. 83, Iss. 1, 2004-01 ,pp. : 28-33

Springer Publishing Company

Access to resources Recommend Favorite