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G Matthijs

Showing results (21-30 of 157) with videos related to

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Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Prenatal diagnosis of trisomy 21 between 1991 and 1999 in the Leuven Centre for Human Genetics: effect of triple test screeningI Witters, E Legius, G Matthijs, et al.
The American Journal of Physiology|July 1, 1990
Effects of substance P on [Ca2+]i and force in intact guinea pig ileal smooth muscleG Matthijs, B Himpens, T L Peeters, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large familyE Legius, E Schollen, G Matthijs, et al.
Acta Clinica Belgica|August 3, 2002
Noniatrogenic haemochromatosis in congenital dyserythropoietic anaemia type II is not related to C282Y and H63D mutations in the HFE gene: report on two brothersW Van Steenbergen, G Matthijs, T Roskams, et al.
Biochimica Et Biophysica Acta|November 26, 1999
Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency)H Carchon, E Van Schaftingen, G Matthijs, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophyH Scheffer, J M Cobben, G Matthijs, et al.
Journal of Inherited Metabolic Disease|October 25, 2008
On the nomenclature of congenital disorders of glycosylation (CDG)J Jaeken, T Hennet, H H Freeze, et al.
Regulatory Peptides|November 1, 1986
Comparison of the biological activity of canine and porcine motilin in rabbitT L Peeters, V Bormans, G Matthijs, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia)E Schollen, S Kjaergaard, E Legius, et al.
Acta Neurologica Belgica|August 10, 2000
Demographic characteristics and prognosis in a Flemish amyotrophic lateral sclerosis populationV Thijs, E Peeters, P Theys, et al.
Pageof 16

Showing results (21-30 of 157) with videos related to

Sort By:
Pageof 16
Genetic Counseling (Geneva, Switzerland)|August 2, 2002
Prenatal diagnosis of trisomy 21 between 1991 and 1999 in the Leuven Centre for Human Genetics: effect of triple test screeningI Witters, E Legius, G Matthijs, et al.
The American Journal of Physiology|July 1, 1990
Effects of substance P on [Ca2+]i and force in intact guinea pig ileal smooth muscleG Matthijs, B Himpens, T L Peeters, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large familyE Legius, E Schollen, G Matthijs, et al.
Acta Clinica Belgica|August 3, 2002
Noniatrogenic haemochromatosis in congenital dyserythropoietic anaemia type II is not related to C282Y and H63D mutations in the HFE gene: report on two brothersW Van Steenbergen, G Matthijs, T Roskams, et al.
Biochimica Et Biophysica Acta|November 26, 1999
Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency)H Carchon, E Van Schaftingen, G Matthijs, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Best practice guidelines for molecular analysis in spinal muscular atrophyH Scheffer, J M Cobben, G Matthijs, et al.
Journal of Inherited Metabolic Disease|October 25, 2008
On the nomenclature of congenital disorders of glycosylation (CDG)J Jaeken, T Hennet, H H Freeze, et al.
Regulatory Peptides|November 1, 1986
Comparison of the biological activity of canine and porcine motilin in rabbitT L Peeters, V Bormans, G Matthijs, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia)E Schollen, S Kjaergaard, E Legius, et al.
Acta Neurologica Belgica|August 10, 2000
Demographic characteristics and prognosis in a Flemish amyotrophic lateral sclerosis populationV Thijs, E Peeters, P Theys, et al.
Pageof 16