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16. Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis. Coetzer T; Palek J; Lawler J; Liu SC; Jarolim P; Lahav M; Prchal JT; Wang W; Alter BP; Schewitz G Blood; 1990 Jun; 75(11):2235-44. PubMed ID: 2346784 [TBL] [Abstract][Full Text] [Related]
17. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity]. Eber SW Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935 [TBL] [Abstract][Full Text] [Related]
18. [Hereditary elliptocytosis in West Africa: frequency and repartition of spectrin variants]. Lecomte MC; Dhermy D; Gautero H; Bournier O; Galand C; Boivin P C R Acad Sci III; 1988; 306(2):43-6. PubMed ID: 3126987 [TBL] [Abstract][Full Text] [Related]
19. The elliptocytoses, ovalocytosis and related disorders. Nurse GT; Coetzer TL; Palek J Baillieres Clin Haematol; 1992 Jan; 5(1):187-207. PubMed ID: 1534499 [No Abstract] [Full Text] [Related]
20. Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis. Dhermy D; Galand C; Bournier O; King MJ; Cynober T; Roberts I; Kanyike F; Adekile A Blood; 1998 Dec; 92(11):4481-2. PubMed ID: 9882098 [No Abstract] [Full Text] [Related] [Next] [New Search]