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Y Le Gall

Showing results (31-40 of 84) with videos related to

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Human Genetics|October 28, 1997
A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutationsA M Jouanolle, P Fergelot, G Gandon, et al.
Atherosclerosis|February 1, 1994
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patientsI Dorval, P Jezequel, C Dubourg, et al.
European Journal of Biochemistry|September 1, 1980
Synthesis of a new reagent, ethyl 4-azidobenzoylaminoacetimidate, and its use for RNA-protein cross-linking within Escherichia coli ribosomal 30-S subunitsR Millon, M Olomucki, J Y Le Gall, et al.
Annales De Biologie Clinique|January 1, 1995
ProteasesJ Nduwimana, L Guenet, I Dorval, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|July 1, 1980
[Measurement of inflammatory activity in chronic rheumatism by blood pretein levels]G Chalès, Y Pawlotsky, A Le Treut, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 8, 1982
Serum lysosomal acid hydrolase activities in Graves' diseaseH Guillou, V David, Y Lorcy, et al.
Gastroenterology|January 29, 1999
Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relativesR Moirand, A M Jouanolle, P Brissot, et al.
Human Molecular Genetics|July 1, 1994
Dinucleotide repeat polymorphism at the D6S510 locusG Gandon, V Lelaure, L Pichon, et al.
Pediatrie|June 1, 1983
[Case of early hydrocephalus in mucopolysaccharidosis type 1]M Roussey, B Le Marec, J Faivre, et al.
Blood Cells, Molecules & Diseases|September 23, 2000
The HFE gene undergoes alternate splicing processesA Thénié, M Orhant, I Gicquel, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
Human Genetics|October 28, 1997
A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutationsA M Jouanolle, P Fergelot, G Gandon, et al.
Atherosclerosis|February 1, 1994
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patientsI Dorval, P Jezequel, C Dubourg, et al.
European Journal of Biochemistry|September 1, 1980
Synthesis of a new reagent, ethyl 4-azidobenzoylaminoacetimidate, and its use for RNA-protein cross-linking within Escherichia coli ribosomal 30-S subunitsR Millon, M Olomucki, J Y Le Gall, et al.
Annales De Biologie Clinique|January 1, 1995
ProteasesJ Nduwimana, L Guenet, I Dorval, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|July 1, 1980
[Measurement of inflammatory activity in chronic rheumatism by blood pretein levels]G Chalès, Y Pawlotsky, A Le Treut, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 8, 1982
Serum lysosomal acid hydrolase activities in Graves' diseaseH Guillou, V David, Y Lorcy, et al.
Gastroenterology|January 29, 1999
Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relativesR Moirand, A M Jouanolle, P Brissot, et al.
Human Molecular Genetics|July 1, 1994
Dinucleotide repeat polymorphism at the D6S510 locusG Gandon, V Lelaure, L Pichon, et al.
Pediatrie|June 1, 1983
[Case of early hydrocephalus in mucopolysaccharidosis type 1]M Roussey, B Le Marec, J Faivre, et al.
Blood Cells, Molecules & Diseases|September 23, 2000
The HFE gene undergoes alternate splicing processesA Thénié, M Orhant, I Gicquel, et al.
Pageof 9