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Katrien Janssens

Showing results (1-10 of 47) with videos related to

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Human Molecular Genetics|September 28, 2002
Molecular genetics of too much boneKatrien Janssens, Wim Van Hul
Prenatal Diagnosis|December 28, 2021
Non-invasive prenatal testing detects blood chimerism in dizygotic twinsEwa Janicki, Katrien Janssens, Bettina Blaumeiser
Placenta|May 14, 2024
The impact of confined placental mosaicism on prenatal cell-free DNA screening: Insights from a monocentric study of 99 casesJessica Rosenblum, Bettina Blaumeiser, Katrien Janssens
Proceedings of the National Academy of Sciences of the United States of America|April 7, 2010
Direct detection of guidance receptor activity during border cell migrationKatrien Janssens, Hsin-Ho Sung, Pernille Rørth
Clinical Case Reports|April 12, 2017
Prenatal homozygosity mapping detects a novel mutation in CHST3 in a fetus with skeletal dysplasia and joint dislocationsJoke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Nature Reviews. Neurology|January 25, 2012
Mechanisms of disease in hereditary sensory and autonomic neuropathiesAnnelies Rotthier, Jonathan Baets, Vincent Timmerman, et al.
Prenatal Diagnosis|August 7, 2024
Monocentric Study on the Performance of Noninvasive Prenatal Testing on Cell-Free DNA for the Detection of Monosomy XKelly Steinfort, Erik Fransen, Bettina Blaumeiser, et al.
Clinical Case Reports|September 5, 2020
Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT eraEvy Vervecken, Bettina Blaumeiser, Tina Vanderheyden, et al.
Endocrine Reviews|May 20, 2005
Transforming growth factor-beta1 to the boneKatrien Janssens, Peter ten Dijke, Sophie Janssens, et al.
Journal of Medical Ethics|September 19, 2019
Chromosomal microarray analysis in prenatal diagnosis: ethical considerations of the Belgian approachJoke Muys, Bettina Blaumeiser, Katrien Janssens, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|September 28, 2002
Molecular genetics of too much boneKatrien Janssens, Wim Van Hul
Prenatal Diagnosis|December 28, 2021
Non-invasive prenatal testing detects blood chimerism in dizygotic twinsEwa Janicki, Katrien Janssens, Bettina Blaumeiser
Placenta|May 14, 2024
The impact of confined placental mosaicism on prenatal cell-free DNA screening: Insights from a monocentric study of 99 casesJessica Rosenblum, Bettina Blaumeiser, Katrien Janssens
Proceedings of the National Academy of Sciences of the United States of America|April 7, 2010
Direct detection of guidance receptor activity during border cell migrationKatrien Janssens, Hsin-Ho Sung, Pernille Rørth
Clinical Case Reports|April 12, 2017
Prenatal homozygosity mapping detects a novel mutation in CHST3 in a fetus with skeletal dysplasia and joint dislocationsJoke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Nature Reviews. Neurology|January 25, 2012
Mechanisms of disease in hereditary sensory and autonomic neuropathiesAnnelies Rotthier, Jonathan Baets, Vincent Timmerman, et al.
Prenatal Diagnosis|August 7, 2024
Monocentric Study on the Performance of Noninvasive Prenatal Testing on Cell-Free DNA for the Detection of Monosomy XKelly Steinfort, Erik Fransen, Bettina Blaumeiser, et al.
Clinical Case Reports|September 5, 2020
Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT eraEvy Vervecken, Bettina Blaumeiser, Tina Vanderheyden, et al.
Endocrine Reviews|May 20, 2005
Transforming growth factor-beta1 to the boneKatrien Janssens, Peter ten Dijke, Sophie Janssens, et al.
Journal of Medical Ethics|September 19, 2019
Chromosomal microarray analysis in prenatal diagnosis: ethical considerations of the Belgian approachJoke Muys, Bettina Blaumeiser, Katrien Janssens, et al.
Pageof 5