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Ophthalmology
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August 31, 2000
Lattice corneal dystrophy
C F Schmitt-Bernard, M Claustres, B Arnaud, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales
|
January 1, 1970
[Human alpha-2 macroglobulin: isolation and composition]
J Demaille, J Broussal, C Colette, et al.
British Journal of Haematology
|
July 1, 1997
Recurrent PIG-A mutation (IVS5+1G-->A) in a paediatric case of paroxysmal nocturnal haemoglobinuria: detection by the protein truncation test
C Maugard, G Margueritte, S Tuffery, et al.
Human Mutation
|
January 1, 1996
A novel mutation (S558X) causing choroideremia
L Beaufrère, S Tuffery, C Hamel, et al.
Human Genetics
|
September 1, 1990
Cystic fibrosis typing with DNA probes and screening for delta F508 deletion in families from southern France
M Claustres, M Desgeorges, P Kjellberg, et al.
FEBS Letters
|
June 1, 1974
Troponins C from reptile and fish muscles and their relation to muscular parvalbumins
J Demaille, E Dutruge, E Eisenberg, et al.
Human Mutation
|
January 1, 1992
Screening for cystic fibrosis mutations in southern France: identification of a frameshift mutation and two missense variations
M Claustres, B Gerrard, P Kjellberg, et al.
Human Mutation
|
June 22, 2000
W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa
C Bareil, V Delague, B Arnaud, et al.
Biochemical and Biophysical Research Communications
|
December 1, 1975
A reappraisal of the relationship of phosphate-acceptor protein to parvalbumins
J Demaille, E Dutruge, G Baron, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles
|
April 27, 1970
[Composition of human alpha 2-macroglobulin isolated by filtration on agarose gel]
J Demaille, J Broussal, C Colette, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 112) with videos related to
Sort By:
Page
of 12
Ophthalmology
|
August 31, 2000
Lattice corneal dystrophy
C F Schmitt-Bernard, M Claustres, B Arnaud, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales
|
January 1, 1970
[Human alpha-2 macroglobulin: isolation and composition]
J Demaille, J Broussal, C Colette, et al.
British Journal of Haematology
|
July 1, 1997
Recurrent PIG-A mutation (IVS5+1G-->A) in a paediatric case of paroxysmal nocturnal haemoglobinuria: detection by the protein truncation test
C Maugard, G Margueritte, S Tuffery, et al.
Human Mutation
|
January 1, 1996
A novel mutation (S558X) causing choroideremia
L Beaufrère, S Tuffery, C Hamel, et al.
Human Genetics
|
September 1, 1990
Cystic fibrosis typing with DNA probes and screening for delta F508 deletion in families from southern France
M Claustres, M Desgeorges, P Kjellberg, et al.
FEBS Letters
|
June 1, 1974
Troponins C from reptile and fish muscles and their relation to muscular parvalbumins
J Demaille, E Dutruge, E Eisenberg, et al.
Human Mutation
|
January 1, 1992
Screening for cystic fibrosis mutations in southern France: identification of a frameshift mutation and two missense variations
M Claustres, B Gerrard, P Kjellberg, et al.
Human Mutation
|
June 22, 2000
W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa
C Bareil, V Delague, B Arnaud, et al.
Biochemical and Biophysical Research Communications
|
December 1, 1975
A reappraisal of the relationship of phosphate-acceptor protein to parvalbumins
J Demaille, E Dutruge, G Baron, et al.
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles
|
April 27, 1970
[Composition of human alpha 2-macroglobulin isolated by filtration on agarose gel]
J Demaille, J Broussal, C Colette, et al.
Page
of 12