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Inge Liebaers

Showing results (31-40 of 60) with videos related to

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Human Reproduction (Oxford, England)|September 28, 2002
Prenatal testing in ICSI pregnancies: incidence of chromosomal anomalies in 1586 karyotypes and relation to sperm parametersMaryse Bonduelle, Elvire Van Assche, Hubert Joris, et al.
Human Mutation|June 21, 2007
A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) regionWilly Lissens, Alessia Arena, Sara Seneca, et al.
Fertility and Sterility|February 6, 2003
Prenatal genetic testing by amniocentesis appears to result in a lower risk of fetal loss than chorionic villus sampling in singleton pregnancies achieved by intracytoplasmic sperm injectionEfstratios Kolibianakis, Kaan Osmanagaoglu, Luc De Catte, et al.
Human Reproduction (Oxford, England)|February 5, 2014
In vitro screening of embryos by whole-genome sequencing: now, in the future or never?Raf Winand, Kristien Hens, Wybo Dondorp, 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.
Molecular Human Reproduction|March 10, 2006
Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriersGonul Ogur, Elvire Van Assche, Walter Vegetti, et al.
European Journal of Human Genetics : EJHG|April 19, 2007
Clinical outcome of preimplantation genetic diagnosis for cystic fibrosis: the Brussels' experienceKathelijn Keymolen, Veerle Goossens, Martine De Rycke, et al.
Nature Protocols|May 10, 2007
Whole-genome multiple displacement amplification from single cellsClaudia Spits, Cédric Le Caignec, Martine De Rycke, et al.
European Journal of Pediatrics|September 1, 2004
Early onset Huntington disease: a neuronal degeneration syndromeSara Seneca, Domique Fagnart, Kathelijn Keymolen, 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.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Human Reproduction (Oxford, England)|September 28, 2002
Prenatal testing in ICSI pregnancies: incidence of chromosomal anomalies in 1586 karyotypes and relation to sperm parametersMaryse Bonduelle, Elvire Van Assche, Hubert Joris, et al.
Human Mutation|June 21, 2007
A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) regionWilly Lissens, Alessia Arena, Sara Seneca, et al.
Fertility and Sterility|February 6, 2003
Prenatal genetic testing by amniocentesis appears to result in a lower risk of fetal loss than chorionic villus sampling in singleton pregnancies achieved by intracytoplasmic sperm injectionEfstratios Kolibianakis, Kaan Osmanagaoglu, Luc De Catte, et al.
Human Reproduction (Oxford, England)|February 5, 2014
In vitro screening of embryos by whole-genome sequencing: now, in the future or never?Raf Winand, Kristien Hens, Wybo Dondorp, 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.
Molecular Human Reproduction|March 10, 2006
Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriersGonul Ogur, Elvire Van Assche, Walter Vegetti, et al.
European Journal of Human Genetics : EJHG|April 19, 2007
Clinical outcome of preimplantation genetic diagnosis for cystic fibrosis: the Brussels' experienceKathelijn Keymolen, Veerle Goossens, Martine De Rycke, et al.
Nature Protocols|May 10, 2007
Whole-genome multiple displacement amplification from single cellsClaudia Spits, Cédric Le Caignec, Martine De Rycke, et al.
European Journal of Pediatrics|September 1, 2004
Early onset Huntington disease: a neuronal degeneration syndromeSara Seneca, Domique Fagnart, Kathelijn Keymolen, 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.
Pageof 6