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British Journal of Haematology
|
November 1, 1993
Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variants
M C Lecomte, M Garbarz, H Gautero, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
October 1, 1996
Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis
M Garbarz, D Bibas, T Cynober, et al.
Journal of Biochemical and Biophysical Methods
|
May 1, 1989
An efficient laboratory made apparatus for DNA amplification
O Bertrand, M H Delfau, M Garbarz, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1983
[Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry]
D Dhermy, C Féo, M Garbarz, et al.
Human Genetics
|
December 1, 1986
Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis
D Dhermy, M Garbarz, M C Lecomte, et al.
British Journal of Haematology
|
April 1, 1990
Severe recessive poikilocytic anaemia with a new spectrin alpha chain variant
M C Lecomte, C Feo, H Gautero, et al.
British Journal of Haematology
|
February 5, 1998
A 5' splice region G-->C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao)
M Garbarz, C Galand, D Bibas, et al.
Blood
|
July 1, 1994
Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site
N Parquet, I Devaux, L Boulanger, et al.
British Journal of Haematology
|
November 1, 1994
A variant of spectrin low-expression allele alpha LELY carrying a hereditary elliptocytosis mutation in codon 28
J Randon, L Boulanger, J Marechal, et al.
British Journal of Haematology
|
July 1, 1995
Ethnic distribution of allele alpha LELY, a low-expression allele of red-cell spectrin alpha-gene
J Maréchal, R Wilmotte, A Kanzaki, et al.
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of 6
Search research articles
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Showing results (21-30 of 56) with videos related to
Sort By:
Page
of 6
British Journal of Haematology
|
November 1, 1993
Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variants
M C Lecomte, M Garbarz, H Gautero, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
October 1, 1996
Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis
M Garbarz, D Bibas, T Cynober, et al.
Journal of Biochemical and Biophysical Methods
|
May 1, 1989
An efficient laboratory made apparatus for DNA amplification
O Bertrand, M H Delfau, M Garbarz, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1983
[Congenital hemolytic anemia with erythrocyte thermal instability and defect of spectrin tetrameric polymerization. Study of erythrocyte deformability in a new case of hereditary pyropoikilocytosis using diffraction viscosimetry]
D Dhermy, C Féo, M Garbarz, et al.
Human Genetics
|
December 1, 1986
Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis
D Dhermy, M Garbarz, M C Lecomte, et al.
British Journal of Haematology
|
April 1, 1990
Severe recessive poikilocytic anaemia with a new spectrin alpha chain variant
M C Lecomte, C Feo, H Gautero, et al.
British Journal of Haematology
|
February 5, 1998
A 5' splice region G-->C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao)
M Garbarz, C Galand, D Bibas, et al.
Blood
|
July 1, 1994
Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site
N Parquet, I Devaux, L Boulanger, et al.
British Journal of Haematology
|
November 1, 1994
A variant of spectrin low-expression allele alpha LELY carrying a hereditary elliptocytosis mutation in codon 28
J Randon, L Boulanger, J Marechal, et al.
British Journal of Haematology
|
July 1, 1995
Ethnic distribution of allele alpha LELY, a low-expression allele of red-cell spectrin alpha-gene
J Maréchal, R Wilmotte, A Kanzaki, et al.
Page
of 6