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Koenraad Devriendt

Showing results (1-10 of 190) with videos related to

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Molecular Syndromology|February 20, 2018
A Novel Missense Variant in the <i>PVRL4</i> Gene Underlying Ectodermal Dysplasia-Syndactyly Syndrome in a Turkish ChildLeila Dardour, Katrien Cosyns, Koenraad Devriendt
The American Journal of Bioethics : AJOB|March 6, 2014
Empirical ethics: the "missing link" in incidental findings recommendationsGabrielle Christenhusz, Koenraad Devriendt, Kris Dierickx
Journal of Clinical Psychopharmacology|March 30, 2018
Low-Dose Aripiprazole and Risperidone for Treating Problem Behavior in Children With Pitt-Hopkins SyndromeSara Lambrechts, Koenraad Devriendt, Annick Vogels
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 17, 2009
Nail-patella syndrome, infantile nephrotic syndrome: complete remission with antiproteinuric treatmentWillem Proesmans, Maria Van Dyck, Koenraad Devriendt
European Journal of Human Genetics : EJHG|May 23, 2013
Secondary variants--in defense of a more fitting term in the incidental findings debateGabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx
Nature Reviews. Genetics|September 16, 2016
Prenatal and pre-implantation genetic diagnosisJoris Robert Vermeesch, Thierry Voet, Koenraad Devriendt
European Journal of Medical Genetics|September 17, 2013
Disclosing incidental findings in genetics contexts: a review of the empirical ethical researchGabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx
European Journal of Human Genetics : EJHG|June 29, 2012
To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contextsGabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx
European Journal of Orthodontics|April 20, 2013
Tooth agenesis patterns and phenotype variation in a cohort of Belgian patients with hypodontia and oligodontia clustered in 79 families with their pedigreesKaroline Dreesen, Steven Swinnen, Koenraad Devriendt, et al.
Ophthalmic Genetics|February 13, 2015
Ophthalmological Findings in 6p Deletion SyndromeTine Cornelis, Maissa Rayyan, Koenraad Devriendt, et al.
Pageof 19

Showing results (1-10 of 190) with videos related to

Sort By:
Pageof 19
Molecular Syndromology|February 20, 2018
A Novel Missense Variant in the <i>PVRL4</i> Gene Underlying Ectodermal Dysplasia-Syndactyly Syndrome in a Turkish ChildLeila Dardour, Katrien Cosyns, Koenraad Devriendt
The American Journal of Bioethics : AJOB|March 6, 2014
Empirical ethics: the "missing link" in incidental findings recommendationsGabrielle Christenhusz, Koenraad Devriendt, Kris Dierickx
Journal of Clinical Psychopharmacology|March 30, 2018
Low-Dose Aripiprazole and Risperidone for Treating Problem Behavior in Children With Pitt-Hopkins SyndromeSara Lambrechts, Koenraad Devriendt, Annick Vogels
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 17, 2009
Nail-patella syndrome, infantile nephrotic syndrome: complete remission with antiproteinuric treatmentWillem Proesmans, Maria Van Dyck, Koenraad Devriendt
European Journal of Human Genetics : EJHG|May 23, 2013
Secondary variants--in defense of a more fitting term in the incidental findings debateGabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx
Nature Reviews. Genetics|September 16, 2016
Prenatal and pre-implantation genetic diagnosisJoris Robert Vermeesch, Thierry Voet, Koenraad Devriendt
European Journal of Medical Genetics|September 17, 2013
Disclosing incidental findings in genetics contexts: a review of the empirical ethical researchGabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx
European Journal of Human Genetics : EJHG|June 29, 2012
To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contextsGabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx
European Journal of Orthodontics|April 20, 2013
Tooth agenesis patterns and phenotype variation in a cohort of Belgian patients with hypodontia and oligodontia clustered in 79 families with their pedigreesKaroline Dreesen, Steven Swinnen, Koenraad Devriendt, et al.
Ophthalmic Genetics|February 13, 2015
Ophthalmological Findings in 6p Deletion SyndromeTine Cornelis, Maissa Rayyan, Koenraad Devriendt, et al.
Pageof 19