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N Gregersen

Showing results (141-150 of 208) with videos related to

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Clinical Genetics|April 1, 1991
Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectivelyS Kølvraa, J Koch, N Gregersen, et al.
Molecular Genetics and Metabolism|February 21, 2006
VLCAD deficiency: pitfalls in newborn screening and confirmation of diagnosis by mutation analysisA Boneh, B S Andresen, N Gregersen, 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.
Journal of Inherited Metabolic Disease|January 1, 1996
The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, C Vianey-Saban, P Bross, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 8, 2000
Characterization of mouse Clpp protease cDNA, gene, and proteinB S Andresen, T J Corydon, M Wilsbech, et al.
The Journal of Pediatrics|June 1, 1985
Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndromeP F Bougnères, F Rocchiccioli, S Kølvraa, et al.
Human Mutation|April 17, 1999
Identification of recurrent and novel mutations in the LDL receptor gene in Spanish patients with familial hypercholesterolemia. Mutations in brief no. 135. OnlineA Cenarro, H K Jensen, E Casao, et al.
Experimental Cell Research|September 1, 1991
Nonradioactive, sequence-specific detection of RNA in situ by primed in situ labeling (PRINS)J Mogensen, S Kølvraa, J Hindkjaer, et al.
Human Mutation|January 1, 1996
Allele-specific measurement of low-density lipoprotein receptor transcript levelsL G Jensen, H K Jensen, F Heath, et al.
Human Heredity|November 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern EuropeN Gregersen, V Winter, D Curtis, et al.
Pageof 21

Showing results (141-150 of 208) with videos related to

Sort By:
Pageof 21
Clinical Genetics|April 1, 1991
Application of fluorescence in situ hybridization techniques in clinical genetics: use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22, respectivelyS Kølvraa, J Koch, N Gregersen, et al.
Molecular Genetics and Metabolism|February 21, 2006
VLCAD deficiency: pitfalls in newborn screening and confirmation of diagnosis by mutation analysisA Boneh, B S Andresen, N Gregersen, 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.
Journal of Inherited Metabolic Disease|January 1, 1996
The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiencyB S Andresen, C Vianey-Saban, P Bross, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 8, 2000
Characterization of mouse Clpp protease cDNA, gene, and proteinB S Andresen, T J Corydon, M Wilsbech, et al.
The Journal of Pediatrics|June 1, 1985
Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndromeP F Bougnères, F Rocchiccioli, S Kølvraa, et al.
Human Mutation|April 17, 1999
Identification of recurrent and novel mutations in the LDL receptor gene in Spanish patients with familial hypercholesterolemia. Mutations in brief no. 135. OnlineA Cenarro, H K Jensen, E Casao, et al.
Experimental Cell Research|September 1, 1991
Nonradioactive, sequence-specific detection of RNA in situ by primed in situ labeling (PRINS)J Mogensen, S Kølvraa, J Hindkjaer, et al.
Human Mutation|January 1, 1996
Allele-specific measurement of low-density lipoprotein receptor transcript levelsL G Jensen, H K Jensen, F Heath, et al.
Human Heredity|November 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern EuropeN Gregersen, V Winter, D Curtis, et al.
Pageof 21