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Annals of Human Genetics|May 1, 1981
Research on molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). Use of new protein mapping and immunological techniquesD Daegelen-Proux, A Kahn, J Marie, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1984
[Sampling, culturing and karyotyping of chorionic villi]Y Rouquet, A Choiset, S Girard, et al.Clinical Genetics|June 1, 1992
Human beta-mannosidosis: a 3-year-old boy with speech impairment and emotional instabilityL Poenaru, S Akli, F Rocchiccioli, et al.European Journal of Pediatrics|April 1, 1988
A variant of mucolipidosis. II. Clinical, biochemical and pathological investigationsL Poenaru, L Castelnau, F Tome, et al.Biochimica Et Biophysica Acta|December 8, 1976
Molecular heterogeneity of rabbit heart phosphorylase kinaseD Daegelen-Proux, M Pierres, Y Alexandre, et al.Human Genetics|January 1, 1985
Lysosomal hydrolase activity in chorionic villi and embryonic cells in cultureL Poenaru, L Castelnau, A Choiset, et al.Clinical Genetics|July 18, 2002
Endothelial nitric oxide synthase gene polymorphisms in Fabry's diseaseC Heltianu, G Costache, K Azibi, et al.Biochimica Et Biophysica Acta|October 12, 1978
Hyperanodic forms of human glucose-6-phosphate dehydrogenaseA Kahn, M Vibert, D Cottreau, et al.Annals of Human Genetics|October 1, 1982
Molecular studies of liver aldolase B in hereditary fructose intolerance using blotting and immunological techniquesC Grégori, F Schapira, A Kahn, et al.Annales De Medecine Interne|January 1, 1985
[Study of hereditary fructose intolerance by methods of molecular biology]J C Dreyfus, F Schapira, C Besmond, et al.Pageof 11