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British Journal of Haematology|October 1, 1988
Occurrence of hereditary spherocytosis and beta thalassaemia in the same family: globin chain synthesis and visco diffractometric studiesB Pautard, C Feo, D Dhermy, et al.Presse Medicale (Paris, France : 1983)|November 26, 1983
[Neonatal hemolysis secondary to congenital poikilocytosis]F Gretillat, N Delepine, D Dhermy, et al.British Journal of Haematology|April 1, 1990
Severe recessive poikilocytic anaemia with a new spectrin alpha chain variantM C Lecomte, C Feo, H Gautero, et al.The Journal of Clinical Investigation|September 1, 1990
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-associationW T Tse, M C Lecomte, F F Costa, et al.The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.Human Genetics|December 1, 1987
Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expressionM C Lecomte, D Dhermy, M Garbarz, et al.Blood|June 1, 1986
Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosisM Garbarz, M C Lecomte, D Dhermy, et al.Prenatal Diagnosis|September 1, 1987
Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrinD Dhermy, C Feo, M Garbarz, et al.Human Genetics|January 1, 1985
Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosisM C Lecomte, D Dhermy, M Garbarz, et al.Pageof 13