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Willy Lissens

Showing results (31-40 of 68) with videos related to

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Fertility and Sterility|June 8, 2006
Preimplantation genetic diagnosis for Marfan syndromeClaudia Spits, Martine De Rycke, Willem Verpoest, et al.
Human Mutation|January 16, 2010
Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer familiesSylvia De Brakeleer, Jacques De Grève, Remy Loris, et al.
International Journal of Andrology|May 20, 2004
Idiopathic non-obstructive azoospermia or severe oligozoospermia: a cross-sectional study in 61 Greek menChariklia Giannouli, Dimitrios G Goulis, Alexander Lambropoulos, et al.
Molecular Human Reproduction|December 11, 2003
Expression pattern of the Y-linked PRY gene suggests a function in apoptosis but not in spermatogenesisKatrien Stouffs, Willy Lissens, Greta Verheyen, et al.
American Journal of Human Genetics|June 9, 2004
Intergenerational instability of the expanded CTG repeat in the DMPK gene: studies in human gametes and preimplantation embryosNele De Temmerman, Karen Sermon, Sara Seneca, et al.
Archives of Neurology|August 16, 2006
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failureAnn Meulemans, Sara Seneca, Lieven Lagae, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN geneKaren Buysse, Sarah Vergult, Silke Mussche, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 16, 2004
Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiencyAnn Meulemans, Willy Lissens, Rudy Van Coster, et al.
Journal of Inherited Metabolic Disease|April 13, 2011
Complex III staining in blue native polyacrylamide gelsJoél Smet, Boel De Paepe, Sara Seneca, et al.
European Journal of Pediatrics|September 1, 2004
Early onset Huntington disease: a neuronal degeneration syndromeSara Seneca, Domique Fagnart, Kathelijn Keymolen, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
Fertility and Sterility|June 8, 2006
Preimplantation genetic diagnosis for Marfan syndromeClaudia Spits, Martine De Rycke, Willem Verpoest, et al.
Human Mutation|January 16, 2010
Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer familiesSylvia De Brakeleer, Jacques De Grève, Remy Loris, et al.
International Journal of Andrology|May 20, 2004
Idiopathic non-obstructive azoospermia or severe oligozoospermia: a cross-sectional study in 61 Greek menChariklia Giannouli, Dimitrios G Goulis, Alexander Lambropoulos, et al.
Molecular Human Reproduction|December 11, 2003
Expression pattern of the Y-linked PRY gene suggests a function in apoptosis but not in spermatogenesisKatrien Stouffs, Willy Lissens, Greta Verheyen, et al.
American Journal of Human Genetics|June 9, 2004
Intergenerational instability of the expanded CTG repeat in the DMPK gene: studies in human gametes and preimplantation embryosNele De Temmerman, Karen Sermon, Sara Seneca, et al.
Archives of Neurology|August 16, 2006
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failureAnn Meulemans, Sara Seneca, Lieven Lagae, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN geneKaren Buysse, Sarah Vergult, Silke Mussche, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 16, 2004
Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiencyAnn Meulemans, Willy Lissens, Rudy Van Coster, et al.
Journal of Inherited Metabolic Disease|April 13, 2011
Complex III staining in blue native polyacrylamide gelsJoél Smet, Boel De Paepe, Sara Seneca, et al.
European Journal of Pediatrics|September 1, 2004
Early onset Huntington disease: a neuronal degeneration syndromeSara Seneca, Domique Fagnart, Kathelijn Keymolen, et al.
Pageof 7