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Karen Grønskov

Showing results (1-10 of 81) with videos related to

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Ophthalmic Genetics|November 1, 2022
<i>RBP4</i>-related eye disease in a Danish family with retinitis pigmentosa and congenital ocular malformationsLine Kessel, Mette Bertelsen, Karen Grønskov
Acta Ophthalmologica|March 12, 2014
Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjectsCecilia Rönnbäck, Karen Grønskov, Michael Larsen
Orphanet Journal of Rare Diseases|November 6, 2007
Oculocutaneous albinismKaren Grønskov, Jakob Ek, Karen Brondum-Nielsen
Ugeskrift for Laeger|October 31, 2006
[Fragile X chromosomes and fragile X syndrome]Susanne Eriksen Boonen, Karen Grønskov, Karen Brøndum-Nielsen
Ophthalmic Genetics|June 9, 2023
Clinical characterization of patients with Kristian Lisbjerg, Mette Bertelsen, Karen Grønskov, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
A nonsense mutation in FMR1 causing fragile X syndromeKaren Grønskov, Karen Brøndum-Nielsen, Alma Dedic, et al.
Ugeskrift for Laeger|March 14, 2012
[The genetic background for the eye malformations anophthalmia and microphthalmia]Laura Sønderberg Roos, Karen Grønskov, Hanne Jensen, et al.
Ophthalmic Genetics|June 11, 2026
A nationwide overview of the clinical and genetic landscape of inherited eye disorders in DenmarkLine Kessel, Mette Kg Andersen, Karen Grønskov, et al.
European Journal of Human Genetics : EJHG|June 17, 2004
Screening of the ARX gene in 682 retarded malesKaren Grønskov, Helle Hjalgrim, Inge-Merete Nielsen, et al.
BMC Research Notes|September 11, 2009
Normal RNAi response in human fragile x fibroblastsCharlotte Madsen, Karen Grønskov, Karen Brøndum-Nielsen, et al.
Pageof 9

Showing results (1-10 of 81) with videos related to

Sort By:
Pageof 9
Ophthalmic Genetics|November 1, 2022
<i>RBP4</i>-related eye disease in a Danish family with retinitis pigmentosa and congenital ocular malformationsLine Kessel, Mette Bertelsen, Karen Grønskov
Acta Ophthalmologica|March 12, 2014
Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjectsCecilia Rönnbäck, Karen Grønskov, Michael Larsen
Orphanet Journal of Rare Diseases|November 6, 2007
Oculocutaneous albinismKaren Grønskov, Jakob Ek, Karen Brondum-Nielsen
Ugeskrift for Laeger|October 31, 2006
[Fragile X chromosomes and fragile X syndrome]Susanne Eriksen Boonen, Karen Grønskov, Karen Brøndum-Nielsen
Ophthalmic Genetics|June 9, 2023
Clinical characterization of patients with Kristian Lisbjerg, Mette Bertelsen, Karen Grønskov, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
A nonsense mutation in FMR1 causing fragile X syndromeKaren Grønskov, Karen Brøndum-Nielsen, Alma Dedic, et al.
Ugeskrift for Laeger|March 14, 2012
[The genetic background for the eye malformations anophthalmia and microphthalmia]Laura Sønderberg Roos, Karen Grønskov, Hanne Jensen, et al.
Ophthalmic Genetics|June 11, 2026
A nationwide overview of the clinical and genetic landscape of inherited eye disorders in DenmarkLine Kessel, Mette Kg Andersen, Karen Grønskov, et al.
European Journal of Human Genetics : EJHG|June 17, 2004
Screening of the ARX gene in 682 retarded malesKaren Grønskov, Helle Hjalgrim, Inge-Merete Nielsen, et al.
BMC Research Notes|September 11, 2009
Normal RNAi response in human fragile x fibroblastsCharlotte Madsen, Karen Grønskov, Karen Brøndum-Nielsen, et al.
Pageof 9