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M Garbarz

Showing results (41-50 of 56) with videos related to

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Human Genetics|February 1, 1993
An alpha-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the alpha v/41 polymorphismN Dalla Venezia, R Wilmotte, L Morlé, 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.
Blood|August 15, 1989
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypesM C Lecomte, M Garbarz, B Grandchamp, 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|April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domainM Garbarz, M C Lecomte, C Féo, et al.
Pediatric 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.
Blood|June 1, 1987
Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosisB Pothier, L Morlé, N Alloisio, et al.
British Journal of Haematology|July 1, 1987
Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemiaB Pothier, L Morlé, N Alloisio, et al.
Blood|August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domainL Morlé, F Morlé, A F Roux, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Human Genetics|February 1, 1993
An alpha-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the alpha v/41 polymorphismN Dalla Venezia, R Wilmotte, L Morlé, 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.
Blood|August 15, 1989
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypesM C Lecomte, M Garbarz, B Grandchamp, 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|April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domainM Garbarz, M C Lecomte, C Féo, et al.
Pediatric 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.
Blood|June 1, 1987
Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosisB Pothier, L Morlé, N Alloisio, et al.
British Journal of Haematology|July 1, 1987
Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemiaB Pothier, L Morlé, N Alloisio, et al.
Blood|August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domainL Morlé, F Morlé, A F Roux, et al.
Pageof 6