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P Guldberg

Showing results (71-80 of 101) with videos related to

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Nucleic Acids Research|April 29, 1998
Detection of mutations in GC-rich DNA by bisulphite denaturing gradient gel electrophoresisP Guldberg, K Grønbak, A Aggerholm, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Brain magnetic resonance imaging in children with optimally controlled hyperphenylalaninaemiaP B Toft, H C Lou, I Krägeloh-Mann, et al.
Oncogene|January 30, 2007
Genomic profiling of malignant melanoma using tiling-resolution arrayCGHG Jönsson, C Dahl, J Staaf, et al.
Journal of Inherited Metabolic Disease|February 22, 2000
Brain phenylalanine concentration in the management of adults with phenylketonuriaR A Moats, R Koch, K Moseley, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Mutation analysis in families with discordant phenotypes of phenylalanine hydroxylase deficiency. Inheritance and expression of the hyperphenylalaninaemiasP Guldberg, H L Levy, R Koch, et al.
The Journal of Pediatrics|September 1, 1994
Maternal mild hyperphenylalaninemia: results of treated and untreated pregnancies in two sistersH L Levy, B S Goss, D K Sullivan, et al.
Atherosclerosis|December 1, 1994
Detection of a single base deletion in codon 424 of the low density lipoprotein receptor gene in a Danish family with familial hypercholesterolemiaH Nissen, A B Hansen, P Guldberg, et al.
Circulation|March 15, 1995
Genetic diagnosis with the denaturing gradient gel electrophoresis technique improves diagnostic precision in familial hypercholesterolemiaH Nissen, A B Hansen, P Guldberg, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 1, 1996
Phenotypic presentation of the FH-Cincinnati type 5 low density lipoprotein receptor mutationH Nissen, A B Hansen, P Guldberg, 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.
Pageof 11

Showing results (71-80 of 101) with videos related to

Sort By:
Pageof 11
Nucleic Acids Research|April 29, 1998
Detection of mutations in GC-rich DNA by bisulphite denaturing gradient gel electrophoresisP Guldberg, K Grønbak, A Aggerholm, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Brain magnetic resonance imaging in children with optimally controlled hyperphenylalaninaemiaP B Toft, H C Lou, I Krägeloh-Mann, et al.
Oncogene|January 30, 2007
Genomic profiling of malignant melanoma using tiling-resolution arrayCGHG Jönsson, C Dahl, J Staaf, et al.
Journal of Inherited Metabolic Disease|February 22, 2000
Brain phenylalanine concentration in the management of adults with phenylketonuriaR A Moats, R Koch, K Moseley, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Mutation analysis in families with discordant phenotypes of phenylalanine hydroxylase deficiency. Inheritance and expression of the hyperphenylalaninaemiasP Guldberg, H L Levy, R Koch, et al.
The Journal of Pediatrics|September 1, 1994
Maternal mild hyperphenylalaninemia: results of treated and untreated pregnancies in two sistersH L Levy, B S Goss, D K Sullivan, et al.
Atherosclerosis|December 1, 1994
Detection of a single base deletion in codon 424 of the low density lipoprotein receptor gene in a Danish family with familial hypercholesterolemiaH Nissen, A B Hansen, P Guldberg, et al.
Circulation|March 15, 1995
Genetic diagnosis with the denaturing gradient gel electrophoresis technique improves diagnostic precision in familial hypercholesterolemiaH Nissen, A B Hansen, P Guldberg, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|February 1, 1996
Phenotypic presentation of the FH-Cincinnati type 5 low density lipoprotein receptor mutationH Nissen, A B Hansen, P Guldberg, 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.
Pageof 11