H Eiberg - JoVE Visualize

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Human Genetics|December 22, 1998

Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1P Koefoed, L Hasholt, K Fenger, et al.

Journal of Medical Genetics|May 2, 2006

Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 geneH Eiberg, L Hansen, B Kjer, et al.

Neurology|May 14, 2003

A novel mutation in the epsilon-sarcoglycan gene causing myoclonus-dystonia syndromeL E Hjermind, L M Werdelin, H Eiberg, et al.

Human Molecular Genetics|September 25, 1997

CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24J E Nielsen, P Koefoed, K Abell, et al.

Clinical Genetics|May 1, 1989

Linkage between serum cholinesterase 2 (CHE2) and gamma-crystallin gene cluster (CRYG): assignment to chromosome 2H Eiberg, L S Nielsen, J Klausen, et al.

Diabetologia|February 22, 2012

Fasting and oral glucose-stimulated levels of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are highly familial traitsA P Gjesing, C T Ekstrøm, H Eiberg, et al.

Journal of Medical Genetics|July 15, 2005

A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2K W Kjaer, H Eiberg, L Hansen, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 9, 1997

Structural organization of the human short-chain acyl-CoA dehydrogenase geneM J Corydon, B S Andresen, P Bross, et al.

British Journal of Cancer|July 1, 2004

Loss of heterozygosity at 9q33 and hypermethylation of the DBCCR1 gene in oral squamous cell carcinomaS Gao, J Worm, P Guldberg, et al.

Genomics|October 1, 1990

Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16M Gardiner, A Sandford, M Deadman, et al.

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Showing results (61-70 of 102) with videos related to

Sort By:

Pageof 11

Human Genetics|December 22, 1998

Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1P Koefoed, L Hasholt, K Fenger, et al.

Journal of Medical Genetics|May 2, 2006

Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 geneH Eiberg, L Hansen, B Kjer, et al.

Neurology|May 14, 2003

A novel mutation in the epsilon-sarcoglycan gene causing myoclonus-dystonia syndromeL E Hjermind, L M Werdelin, H Eiberg, et al.

Human Molecular Genetics|September 25, 1997

CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24J E Nielsen, P Koefoed, K Abell, et al.

Clinical Genetics|May 1, 1989

Linkage between serum cholinesterase 2 (CHE2) and gamma-crystallin gene cluster (CRYG): assignment to chromosome 2H Eiberg, L S Nielsen, J Klausen, et al.

Diabetologia|February 22, 2012

Fasting and oral glucose-stimulated levels of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are highly familial traitsA P Gjesing, C T Ekstrøm, H Eiberg, et al.

Journal of Medical Genetics|July 15, 2005

A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2K W Kjaer, H Eiberg, L Hansen, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 9, 1997

Structural organization of the human short-chain acyl-CoA dehydrogenase geneM J Corydon, B S Andresen, P Bross, et al.

British Journal of Cancer|July 1, 2004

Loss of heterozygosity at 9q33 and hypermethylation of the DBCCR1 gene in oral squamous cell carcinomaS Gao, J Worm, P Guldberg, et al.

Genomics|October 1, 1990

Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16M Gardiner, A Sandford, M Deadman, et al.

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