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P Guldberg

Showing results (21-30 of 101) with videos related to

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Human Mutation|January 1, 1996
Phenylalanine hydroxylase deficiency in a population in Germany: mutational profile and nine novel mutationsP Guldberg, R Mallmann, K F Henriksen, et al.
Ugeskrift for Laeger|June 16, 1997
[Hemoglobinopathy in the county of Copenhagen]H S Birgens, H Karle, P Guldberg, et al.
Journal of Medical Genetics|March 4, 2000
Mutation analysis in glutaric aciduria type IJ Zschocke, E Quak, P Guldberg, et al.
Methods in Molecular Medicine|February 11, 2012
T-cell receptor clonotype mapping using denaturing gradient gel electrophoresis : analysis of clonal T-cell responses in melanomaP T Straten, J C Becker, J Zeuthen, et al.
The Journal of Investigative Dermatology|April 4, 2000
Anti-melanocyte T cell responses - methodology versus biologyP thor Straten, P Guldberg, U Moerch, et al.
Biochemical and Molecular Medicine|April 1, 1997
The relationship of genotype to phenotype in phenylalanine hydroxylase deficiencyR Koch, K Fishler, C Azen, et al.
Cancer Immunology, Immunotherapy : CII|September 29, 1999
In situ T cells in melanomaP thor Straten, J C Becker, P Guldberg, et al.
Genomics|September 1, 1992
Molecular basis for nonphenylketonuria hyperphenylalaninemiaE Economou-Petersen, K F Henriksen, P Guldberg, et al.
Pediatrics|November 4, 2000
Blood-brain phenylalanine relationships in persons with phenylketonuriaR Koch, R Moats, F Guttler, et al.
Journal of Medical Genetics|February 1, 1996
Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counsellingP Guldberg, H L Levy, K F Henriksen, et al.
Pageof 11

Showing results (21-30 of 101) with videos related to

Sort By:
Pageof 11
Human Mutation|January 1, 1996
Phenylalanine hydroxylase deficiency in a population in Germany: mutational profile and nine novel mutationsP Guldberg, R Mallmann, K F Henriksen, et al.
Ugeskrift for Laeger|June 16, 1997
[Hemoglobinopathy in the county of Copenhagen]H S Birgens, H Karle, P Guldberg, et al.
Journal of Medical Genetics|March 4, 2000
Mutation analysis in glutaric aciduria type IJ Zschocke, E Quak, P Guldberg, et al.
Methods in Molecular Medicine|February 11, 2012
T-cell receptor clonotype mapping using denaturing gradient gel electrophoresis : analysis of clonal T-cell responses in melanomaP T Straten, J C Becker, J Zeuthen, et al.
The Journal of Investigative Dermatology|April 4, 2000
Anti-melanocyte T cell responses - methodology versus biologyP thor Straten, P Guldberg, U Moerch, et al.
Biochemical and Molecular Medicine|April 1, 1997
The relationship of genotype to phenotype in phenylalanine hydroxylase deficiencyR Koch, K Fishler, C Azen, et al.
Cancer Immunology, Immunotherapy : CII|September 29, 1999
In situ T cells in melanomaP thor Straten, J C Becker, P Guldberg, et al.
Genomics|September 1, 1992
Molecular basis for nonphenylketonuria hyperphenylalaninemiaE Economou-Petersen, K F Henriksen, P Guldberg, et al.
Pediatrics|November 4, 2000
Blood-brain phenylalanine relationships in persons with phenylketonuriaR Koch, R Moats, F Guttler, et al.
Journal of Medical Genetics|February 1, 1996
Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counsellingP Guldberg, H L Levy, K F Henriksen, et al.
Pageof 11