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W Lissens

Showing results (61-70 of 195) with videos related to

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Blood|January 1, 1994
Antithrombin-Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosisK Jochmans, W Lissens, R Vervoort, et al.
International Journal of Bio-Medical Computing|December 1, 1988
Computer aided phenotyping of dyslipoproteinemiaH Pincé, C Cobbaert, M van de Woestijne, et al.
Human Reproduction (Oxford, England)|January 13, 2012
Array comparative genomic hybridization in male infertilityK Stouffs, D Vandermaelen, A Massart, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Localization by fluorescence in situ hybridization of the human functional beta-glucuronidase gene (GUSB) to 7q11.21 --> q11.22 and two pseudogenes to 5p13 and 5q13F Speleman, R Vervoort, N van Roy, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosisS Seneca, M Abramowicz, W Lissens, et al.
Molecular Human Reproduction|June 23, 2001
Characterization of the genomic organization, localization and expression of four PRY genes (PRY1, PRY2, PRY3 and PRY4)K Stouffs, W Lissens, L Van Landuyt, et al.
Molecular Human Reproduction|March 24, 2000
Validation of a simple Yq deletion screening programme in an ICSI candidate populationL Van Landuyt, W Lissens, K Stouffs, et al.
Clinical Genetics|November 13, 2010
Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutationA Fiumara, R Barone, A Arena, et al.
Journal of Hypertension|August 1, 1988
Erythrocyte and leucocyte sodium and potassium transport systems during long-term diuretic administration in menP Lijnen, P Hespel, R Fagard, et al.
Methods and Findings in Experimental and Clinical Pharmacology|October 1, 1985
Differential responses of plasma aldosterone, cortisol and adrenocorticotropin to two dopamine receptor antagonistsJ Staessen, R Fiocchi, R Bouillon, et al.
Pageof 20

Showing results (61-70 of 195) with videos related to

Sort By:
Pageof 20
Blood|January 1, 1994
Antithrombin-Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosisK Jochmans, W Lissens, R Vervoort, et al.
International Journal of Bio-Medical Computing|December 1, 1988
Computer aided phenotyping of dyslipoproteinemiaH Pincé, C Cobbaert, M van de Woestijne, et al.
Human Reproduction (Oxford, England)|January 13, 2012
Array comparative genomic hybridization in male infertilityK Stouffs, D Vandermaelen, A Massart, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Localization by fluorescence in situ hybridization of the human functional beta-glucuronidase gene (GUSB) to 7q11.21 --> q11.22 and two pseudogenes to 5p13 and 5q13F Speleman, R Vervoort, N van Roy, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosisS Seneca, M Abramowicz, W Lissens, et al.
Molecular Human Reproduction|June 23, 2001
Characterization of the genomic organization, localization and expression of four PRY genes (PRY1, PRY2, PRY3 and PRY4)K Stouffs, W Lissens, L Van Landuyt, et al.
Molecular Human Reproduction|March 24, 2000
Validation of a simple Yq deletion screening programme in an ICSI candidate populationL Van Landuyt, W Lissens, K Stouffs, et al.
Clinical Genetics|November 13, 2010
Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutationA Fiumara, R Barone, A Arena, et al.
Journal of Hypertension|August 1, 1988
Erythrocyte and leucocyte sodium and potassium transport systems during long-term diuretic administration in menP Lijnen, P Hespel, R Fagard, et al.
Methods and Findings in Experimental and Clinical Pharmacology|October 1, 1985
Differential responses of plasma aldosterone, cortisol and adrenocorticotropin to two dopamine receptor antagonistsJ Staessen, R Fiocchi, R Bouillon, et al.
Pageof 20