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Koenraad Devriendt

Showing results (11-20 of 190) with videos related to

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Retinal Cases & Brief Reports|August 19, 2017
SEVERE CASE OF RENAL COLOBOMA SYNDROME IN LONG-TERM FOLLOW-UPLise Sels, Werner Dirven, Koenraad Devriendt, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an exampleVeerle De Wolf, Nathalie Brison, Koenraad Devriendt, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Isolated terminal limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome and ARHGAP31 mutationsMala Isrie, Wim Wuyts, Hilde Van Esch, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
Why genomics shouldn't get too personal: in favor of filters: Re: invited comment by Holly K. Tabor et al. in American Journal of Medical Genetics Part A Volume 155Gabrielle M Christenhusz, Koenraad Devriendt, Joris Vermeesch, et al.
American Journal of Medical Genetics. Part A|June 29, 2012
Haploinsufficiency of elastin gene may lead to familial cardiopathy and pulmonary emphysemaJacoba J Louw, Geert Verleden, Marc Gewillig, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
Middle and inner ear malformations in velocardiofacial syndromeKoenraad Devriendt, Ann Swillen, Isabelle Schatteman, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 10, 2012
Array-based approaches in prenatal diagnosisPaul D Brady, Koenraad Devriendt, Jan Deprest, et al.
Medicine, Health Care, and Philosophy|November 20, 2014
Ethical signposts for clinical geneticists in secondary variant and incidental finding disclosure discussionsGabrielle M Christenhusz, Koenraad Devriendt, Hilde Van Esch, et al.
European Journal of Medical Genetics|February 10, 2015
Focus group discussions on secondary variants and next-generation sequencing technologiesGabrielle M Christenhusz, Koenraad Devriendt, Hilde Van Esch, et al.
Human Genetics|September 21, 2004
Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletionMorten Dunø, Hanne Hove, Maria Kirchhoff, et al.
Pageof 19

Showing results (11-20 of 190) with videos related to

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Pageof 19
Retinal Cases & Brief Reports|August 19, 2017
SEVERE CASE OF RENAL COLOBOMA SYNDROME IN LONG-TERM FOLLOW-UPLise Sels, Werner Dirven, Koenraad Devriendt, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an exampleVeerle De Wolf, Nathalie Brison, Koenraad Devriendt, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Isolated terminal limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome and ARHGAP31 mutationsMala Isrie, Wim Wuyts, Hilde Van Esch, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
Why genomics shouldn't get too personal: in favor of filters: Re: invited comment by Holly K. Tabor et al. in American Journal of Medical Genetics Part A Volume 155Gabrielle M Christenhusz, Koenraad Devriendt, Joris Vermeesch, et al.
American Journal of Medical Genetics. Part A|June 29, 2012
Haploinsufficiency of elastin gene may lead to familial cardiopathy and pulmonary emphysemaJacoba J Louw, Geert Verleden, Marc Gewillig, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
Middle and inner ear malformations in velocardiofacial syndromeKoenraad Devriendt, Ann Swillen, Isabelle Schatteman, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 10, 2012
Array-based approaches in prenatal diagnosisPaul D Brady, Koenraad Devriendt, Jan Deprest, et al.
Medicine, Health Care, and Philosophy|November 20, 2014
Ethical signposts for clinical geneticists in secondary variant and incidental finding disclosure discussionsGabrielle M Christenhusz, Koenraad Devriendt, Hilde Van Esch, et al.
European Journal of Medical Genetics|February 10, 2015
Focus group discussions on secondary variants and next-generation sequencing technologiesGabrielle M Christenhusz, Koenraad Devriendt, Hilde Van Esch, et al.
Human Genetics|September 21, 2004
Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletionMorten Dunø, Hanne Hove, Maria Kirchhoff, et al.
Pageof 19