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The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.British Journal of Haematology|July 1, 1997
Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defectsD Dhermy, C Galand, O Bournier, 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.European Journal of Pediatrics|May 18, 1979
A girl with an end-to-end fusion of two X'SC Stoll, C Lausecker, A PennerathPediatric Research|October 1, 1984
Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemiaD Dhermy, M C Lecomte, M Garbarz, et al.Transgenic Research|November 1, 1992
Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin geneG Grimber, C Galand, M Garbarz, et al.Human Genetics|May 19, 1976
[A girl with a deletion (2) (q34q36): cytogenetic and clinical observations (author's transl)]S Warter, C Lausecker, A PennerathBritish Journal of Haematology|February 1, 1992
Elliptocytosis-associated spectrin Rouen (beta 220/218) has a truncated but still phosphorylatable beta chainM C Lecomte, H Gautero, O Bournier, et al.Journal D'Urologie|January 1, 1982
[Spontaneous regression of a dolichomegaureter in a 4-month-old child]C Viville, R de Petriconi, C LauseckerLa Nouvelle Presse Medicale|July 3, 1982
[Hereditary diseases of the human erythrocyte membrane skeleton (author's transl)]P BoivinPageof 34