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M Garbarz

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Blood|August 15, 1992
Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin geneM Garbarz, L Boulanger, S Pedroni, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 casesD Dhermy, M Garbarz, M C Lecomte, et al.
Blood|November 1, 1984
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosisM Garbarz, D Dhermy, M C Lecomte, et al.
The Journal of Clinical Investigation|July 1, 1991
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutationM Garbarz, W T Tse, P G Gallagher, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1989
[Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant]M Garbarz, I Devaux, B Grandchamp, 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.
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.
The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Blood|August 15, 1992
Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin geneM Garbarz, L Boulanger, S Pedroni, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 casesD Dhermy, M Garbarz, M C Lecomte, et al.
Blood|November 1, 1984
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosisM Garbarz, D Dhermy, M C Lecomte, et al.
The Journal of Clinical Investigation|July 1, 1991
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutationM Garbarz, W T Tse, P G Gallagher, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1989
[Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant]M Garbarz, I Devaux, B Grandchamp, 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.
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.
The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.
Pageof 6