H G Eiken - JoVE Visualize

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European Journal of Pediatrics|December 10, 1997

Pituitary dwarfism in the R271W Pit-1 gene mutationD Aarskog, H G Eiken, R Bjerknes, et al.

Human Genetics|August 1, 1997

Phenylketonuria and the peoples of Northern IrelandJ Zschocke, J P Mallory, H G Eiken, et al.

The European Respiratory Journal|April 6, 2006

Genetic association between COPD and polymorphisms in TNF, ADRB2 and EPHX1J Brøgger, V M Steen, H G Eiken, et al.

Human Genetics|February 1, 1995

The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzymeP M Knappskog, H G Eiken, A Martinez, et al.

European Journal of Pediatrics|July 1, 1996

Phenylketonuria genotypes correlated to metabolic phenotype groups in NorwayH G Eiken, P M Knappskog, K Motzfeldt, et al.

FEBS Letters|April 25, 1988

A zebrafish engrailed-like homeobox sequence expressed during embryogenesisA Fjose, H G Eiken, P R Njølstad, et al.

Human Mutation|January 1, 1992

A de novo phenylketonuria mutation: ATG (Met) to ATA (Ile) in the start codon of the phenylalanine hydroxylase geneH G Eiken, P M Knappskog, J Apold, et al.

Human Genetics|March 1, 1992

PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions and phenotype characteristicsH G Eiken, K Stangeland, L Skjelkvåle, et al.

Nucleic Acids Research|April 11, 1991

Application of natural and amplification created restriction sites for the diagnosis of PKU mutationsH G Eiken, E Odland, H Boman, et al.

Human Mutation|January 1, 1996

PKU mutation (D143G) associated with an apparent high residual enzyme activity: expression of a kinetic variant form of phenylalanine hydroxylase in three different systemsP M Knappskog, H G Eiken, A Martínez, et al.

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Showing results (11-20 of 38) with videos related to

Sort By:

Pageof 4

European Journal of Pediatrics|December 10, 1997

Pituitary dwarfism in the R271W Pit-1 gene mutationD Aarskog, H G Eiken, R Bjerknes, et al.

Human Genetics|August 1, 1997

Phenylketonuria and the peoples of Northern IrelandJ Zschocke, J P Mallory, H G Eiken, et al.

The European Respiratory Journal|April 6, 2006

Genetic association between COPD and polymorphisms in TNF, ADRB2 and EPHX1J Brøgger, V M Steen, H G Eiken, et al.

Human Genetics|February 1, 1995

The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzymeP M Knappskog, H G Eiken, A Martinez, et al.

European Journal of Pediatrics|July 1, 1996

Phenylketonuria genotypes correlated to metabolic phenotype groups in NorwayH G Eiken, P M Knappskog, K Motzfeldt, et al.

FEBS Letters|April 25, 1988

A zebrafish engrailed-like homeobox sequence expressed during embryogenesisA Fjose, H G Eiken, P R Njølstad, et al.

Human Mutation|January 1, 1992

A de novo phenylketonuria mutation: ATG (Met) to ATA (Ile) in the start codon of the phenylalanine hydroxylase geneH G Eiken, P M Knappskog, J Apold, et al.

Human Genetics|March 1, 1992

PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions and phenotype characteristicsH G Eiken, K Stangeland, L Skjelkvåle, et al.

Nucleic Acids Research|April 11, 1991

Application of natural and amplification created restriction sites for the diagnosis of PKU mutationsH G Eiken, E Odland, H Boman, et al.

Human Mutation|January 1, 1996

PKU mutation (D143G) associated with an apparent high residual enzyme activity: expression of a kinetic variant form of phenylalanine hydroxylase in three different systemsP M Knappskog, H G Eiken, A Martínez, et al.

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