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G Matthijs

Showing results (61-70 of 157) with videos related to

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FEBS Letters|July 1, 1999
Effect of mutations found in carbohydrate-deficient glycoprotein syndrome type IA on the activity of phosphomannomutase 2M Pirard, G Matthijs, L Heykants, et al.
Neurology|November 1, 1996
D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosisW Robberecht, T Aguirre, L Van den Bosch, et al.
Genomics|February 15, 1997
PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13G Matthijs, E Schollen, M Pirard, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Prenatal diagnosis in CDG1 families: beware of heterogeneityG Matthijs, E Schollen, J J Cassiman, et al.
Human Mutation|May 29, 1998
Fluorescent chemical cleavage of mismatches for efficient screening of the factor VIII geneK Freson, K Peerlinck, T Aguirre, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardationM Tabaku, E Legius, W Robberecht, et al.
Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.
Annales De Genetique|January 1, 1997
Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?K Devriendt, G Naulaers, G Matthijs, et al.
Biomaterials|March 29, 2000
Characterization of protein-resistant dextran monolayersR A Frazie, G Matthijs, M C Davies, et al.
DNA and Cell Biology|July 1, 1994
Cloning and characterization of the promoter region of the murine alpha-4 integrin subunitC De Meirsman, E Schollen, M Jaspers, et al.
Pageof 16

Showing results (61-70 of 157) with videos related to

Sort By:
Pageof 16
FEBS Letters|July 1, 1999
Effect of mutations found in carbohydrate-deficient glycoprotein syndrome type IA on the activity of phosphomannomutase 2M Pirard, G Matthijs, L Heykants, et al.
Neurology|November 1, 1996
D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosisW Robberecht, T Aguirre, L Van den Bosch, et al.
Genomics|February 15, 1997
PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13G Matthijs, E Schollen, M Pirard, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Prenatal diagnosis in CDG1 families: beware of heterogeneityG Matthijs, E Schollen, J J Cassiman, et al.
Human Mutation|May 29, 1998
Fluorescent chemical cleavage of mismatches for efficient screening of the factor VIII geneK Freson, K Peerlinck, T Aguirre, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardationM Tabaku, E Legius, W Robberecht, et al.
Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.
Annales De Genetique|January 1, 1997
Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?K Devriendt, G Naulaers, G Matthijs, et al.
Biomaterials|March 29, 2000
Characterization of protein-resistant dextran monolayersR A Frazie, G Matthijs, M C Davies, et al.
DNA and Cell Biology|July 1, 1994
Cloning and characterization of the promoter region of the murine alpha-4 integrin subunitC De Meirsman, E Schollen, M Jaspers, et al.
Pageof 16