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Lilian Bomme Ousager

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Clinical Dysmorphology|May 29, 2009
Two siblings with microcephaly, growth retardation, cataract, hearing loss, and unusual appearanceLars Kjaersgaard Hansen, Anette Bygum, Lilian Bomme Ousager
Ugeskrift for Laeger|February 27, 2010
[Dravet syndrome]Lars Kjaersgård Hansen, Niels Henrik Rasmussen, Lilian Bomme Ousager
Ugeskrift for Laeger|February 27, 2010
[Dravet syndrome diagnostics]Lars Kjaersgård Hansen, Niels Henrik Rasmussen, Lilian Bomme Ousager
European Journal of Human Genetics : EJHG|January 22, 2015
Research participants in NGS studies want to know about incidental findingsAnne Marie Jelsig, Niels Qvist, Klaus Brusgaard, et al.
Ugeskrift for Laeger|October 28, 2014
[Hereditary palmoplantar keratoderma - a focus on clinical and molecular genetic aspects]Shailajah Kamaleswaran, Lilian Bomme Ousager, Rasmus Overgaard Bach, et al.
Ugeskrift for Laeger|March 10, 2023
Stine Bjørn Gram, Klaus Brusgaard, Lilian Bomme Ousager, et al.
Diseases of the Colon and Rectum|July 8, 2016
Juvenile Polyps in Denmark From 1995 to 2014Anne Marie Jelsig, Lilian Bomme Ousager, Klaus Brusgaard, et al.
Ugeskrift for Laeger|December 16, 2014
[Early-onset epileptic encephalopathy caused by CDKL5 mutation]Helle Hjalmgrim, Lars Kjærsgaard Hansen, Lilian Bomme Ousager, et al.
Molecular Genetics & Genomic Medicine|December 16, 2017
ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasiaPernille M Tørring, Anette D Kjeldsen, Lilian Bomme Ousager, et al.
European Journal of Medical Genetics|November 21, 2016
Novel ELN mutation in a family with supravalvular aortic stenosis and intracranial aneurysmAnne Marie Jelsig, Zsolt Urban, Vishwanathan Hucthagowder, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Clinical Dysmorphology|May 29, 2009
Two siblings with microcephaly, growth retardation, cataract, hearing loss, and unusual appearanceLars Kjaersgaard Hansen, Anette Bygum, Lilian Bomme Ousager
Ugeskrift for Laeger|February 27, 2010
[Dravet syndrome]Lars Kjaersgård Hansen, Niels Henrik Rasmussen, Lilian Bomme Ousager
Ugeskrift for Laeger|February 27, 2010
[Dravet syndrome diagnostics]Lars Kjaersgård Hansen, Niels Henrik Rasmussen, Lilian Bomme Ousager
European Journal of Human Genetics : EJHG|January 22, 2015
Research participants in NGS studies want to know about incidental findingsAnne Marie Jelsig, Niels Qvist, Klaus Brusgaard, et al.
Ugeskrift for Laeger|October 28, 2014
[Hereditary palmoplantar keratoderma - a focus on clinical and molecular genetic aspects]Shailajah Kamaleswaran, Lilian Bomme Ousager, Rasmus Overgaard Bach, et al.
Ugeskrift for Laeger|March 10, 2023
Stine Bjørn Gram, Klaus Brusgaard, Lilian Bomme Ousager, et al.
Diseases of the Colon and Rectum|July 8, 2016
Juvenile Polyps in Denmark From 1995 to 2014Anne Marie Jelsig, Lilian Bomme Ousager, Klaus Brusgaard, et al.
Ugeskrift for Laeger|December 16, 2014
[Early-onset epileptic encephalopathy caused by CDKL5 mutation]Helle Hjalmgrim, Lars Kjærsgaard Hansen, Lilian Bomme Ousager, et al.
Molecular Genetics & Genomic Medicine|December 16, 2017
ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasiaPernille M Tørring, Anette D Kjeldsen, Lilian Bomme Ousager, et al.
European Journal of Medical Genetics|November 21, 2016
Novel ELN mutation in a family with supravalvular aortic stenosis and intracranial aneurysmAnne Marie Jelsig, Zsolt Urban, Vishwanathan Hucthagowder, et al.
Pageof 5