H Eiberg - JoVE Visualize

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European Journal of Human Genetics : EJHG|July 4, 2001

Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigreeG Kitsos, H Eiberg, E Economou-Petersen, et al.

Nature|November 4, 1985

Localization of cystic fibrosis locus to human chromosome 7cen-q22B J Wainwright, P J Scambler, J Schmidtke, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 1998

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic studyJ E Nielsen, K Krabbe, P Jennum, et al.

Science (New York, N.Y.)|November 29, 1985

Cystic fibrosis locus defined by a genetically linked polymorphic DNA markerL C Tsui, M Buchwald, D Barker, et al.

American Journal of Medical Genetics. Part A|July 13, 2012

Genetic studies in congenital anterior midline cervical cleftL P Jakobsen, P Pfeiffer, M Andersen, et al.

Diabetes|July 25, 2000

NeuroD/BETA2 gene variability and diabetes: no associations to late-onset type 2 diabetes but an A45 allele may represent a susceptibility marker for type 1 diabetes among Danes. Danish Study Group of Diabetes in Childhood, and the Danish IDDM Epidemiology and Genetics GroupL Hansen, J N Jensen, S Urioste, et al.

Genomics|September 1, 1990

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneityG J Farrar, P McWilliam, D G Bradley, et al.

Molecular Genetics and Metabolism|June 5, 1999

A polymorphic variant in the human electron transfer flavoprotein alpha-chain (alpha-T171) displays decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentationP Bross, P Pedersen, V Winter, et al.

Genes and Immunity|January 26, 2007

Deficiency of mannan-binding lectin associated serine protease-2 due to missense polymorphismsS Thiel, R Steffensen, I J Christensen, et al.

Diabetologia|September 24, 1999

Hepatocyte nuclear factor-6: associations between genetic variability and type II diabetes and between genetic variability and estimates of insulin secretionA M Møller, J Ek, S M Durviaux, et al.

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Showing results (81-90 of 102) with videos related to

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Pageof 11

European Journal of Human Genetics : EJHG|July 4, 2001

Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigreeG Kitsos, H Eiberg, E Economou-Petersen, et al.

Nature|November 4, 1985

Localization of cystic fibrosis locus to human chromosome 7cen-q22B J Wainwright, P J Scambler, J Schmidtke, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 1998

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic studyJ E Nielsen, K Krabbe, P Jennum, et al.

Science (New York, N.Y.)|November 29, 1985

Cystic fibrosis locus defined by a genetically linked polymorphic DNA markerL C Tsui, M Buchwald, D Barker, et al.

American Journal of Medical Genetics. Part A|July 13, 2012

Genetic studies in congenital anterior midline cervical cleftL P Jakobsen, P Pfeiffer, M Andersen, et al.

Diabetes|July 25, 2000

NeuroD/BETA2 gene variability and diabetes: no associations to late-onset type 2 diabetes but an A45 allele may represent a susceptibility marker for type 1 diabetes among Danes. Danish Study Group of Diabetes in Childhood, and the Danish IDDM Epidemiology and Genetics GroupL Hansen, J N Jensen, S Urioste, et al.

Genomics|September 1, 1990

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneityG J Farrar, P McWilliam, D G Bradley, et al.

Molecular Genetics and Metabolism|June 5, 1999

A polymorphic variant in the human electron transfer flavoprotein alpha-chain (alpha-T171) displays decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentationP Bross, P Pedersen, V Winter, et al.

Genes and Immunity|January 26, 2007

Deficiency of mannan-binding lectin associated serine protease-2 due to missense polymorphismsS Thiel, R Steffensen, I J Christensen, et al.

Diabetologia|September 24, 1999

Hepatocyte nuclear factor-6: associations between genetic variability and type II diabetes and between genetic variability and estimates of insulin secretionA M Møller, J Ek, S M Durviaux, et al.

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