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I Maire

Showing results (71-80 of 121) with videos related to

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Journal De Genetique Humaine|March 1, 1979
[Mucopolysaccharidesis Type VII resulting from beta-glucuronidase deficiency. Report of one family]P Guibaud, I Maire, R Goddon, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Genetic heterogeneity of the GLDC gene in 28 unrelated patients with glycine encephalopathyC Conter, M O Rolland, D Cheillan, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Glycogen storage disease type IV presenting as hydrops fetalisA Alegria, E Martins, M Dias, et al.
Human Mutation|January 1, 1996
A 5-megabase familial deletion removes the IDS and FMR-1 genes in a male Hunter patientA M Birot, B Delobel, P Gronnier, et al.
The Journal of Pediatrics|August 1, 1989
Glycogen storage disease and inflammatory bowel diseaseL de Parscau, I Maire, P Guibaud, et al.
Pediatrie|October 1, 1982
[Type II fucosidosis. 2 cases]B Echenne, P Baldet, I Maire, et al.
Journal of Medical Genetics|April 5, 2005
Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in uteroR Froissart, D Cheillan, R Bouvier, et al.
Annales De Medecine Interne|January 1, 1991
[Another etiology of intermittent claudication of the jaw: Mac Ardle's disease (muscular glycogenosis type V)]J L Dupond, I Maire, B De Wazières, et al.
Revue Neurologique|January 1, 1991
[Mannosidosis type II]C Tranchant, J Reis, J L Dietemann, et al.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|November 1, 1995
Usefulness of reference materials in calibration of enzyme activitiesJ M Lessinger, G Férard, D Grafmeyer, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Journal De Genetique Humaine|March 1, 1979
[Mucopolysaccharidesis Type VII resulting from beta-glucuronidase deficiency. Report of one family]P Guibaud, I Maire, R Goddon, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Genetic heterogeneity of the GLDC gene in 28 unrelated patients with glycine encephalopathyC Conter, M O Rolland, D Cheillan, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Glycogen storage disease type IV presenting as hydrops fetalisA Alegria, E Martins, M Dias, et al.
Human Mutation|January 1, 1996
A 5-megabase familial deletion removes the IDS and FMR-1 genes in a male Hunter patientA M Birot, B Delobel, P Gronnier, et al.
The Journal of Pediatrics|August 1, 1989
Glycogen storage disease and inflammatory bowel diseaseL de Parscau, I Maire, P Guibaud, et al.
Pediatrie|October 1, 1982
[Type II fucosidosis. 2 cases]B Echenne, P Baldet, I Maire, et al.
Journal of Medical Genetics|April 5, 2005
Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in uteroR Froissart, D Cheillan, R Bouvier, et al.
Annales De Medecine Interne|January 1, 1991
[Another etiology of intermittent claudication of the jaw: Mac Ardle's disease (muscular glycogenosis type V)]J L Dupond, I Maire, B De Wazières, et al.
Revue Neurologique|January 1, 1991
[Mannosidosis type II]C Tranchant, J Reis, J L Dietemann, et al.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|November 1, 1995
Usefulness of reference materials in calibration of enzyme activitiesJ M Lessinger, G Férard, D Grafmeyer, et al.
Pageof 13