Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Guldberg

Showing results (1-10 of 101) with videos related to

Pageof 11
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1994
Mutation screening versus gene scanning for genotyping phenylketonuria patientsP Guldberg, F Güttler
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutations in the phenylalanine hydroxylase gene: genetic determinants for the phenotypic variability of hyperphenylalaninemiaF Güttler, P Guldberg
Nucleic Acids Research|March 11, 1994
'Broad-range' DGGE for single-step mutation scanning of entire genes: application to human phenylalanine hydroxylase geneP Guldberg, F Güttler
Nucleic Acids Research|May 11, 1993
A simple method for identification of point mutations using denaturing gradient gel electrophoresisP Guldberg, F Güttler
European Journal of Pediatrics|July 1, 1996
The influence of mutations of enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiencyF Güttler, P Guldberg
Annals of Medicine|June 1, 1992
PCR in the diagnosis of phenylketonuriaP Guldberg, F Güttler
European Journal of Pediatrics|October 24, 2000
Mutation analysis anticipates dietary requirements in phenylketonuriaF Güttler, P Guldberg
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutations in the phenylalanine hydroxylase gene: methods for their characterizationP Guldberg, F Güttler
Clinical Chemistry|June 28, 2001
In-tube DNA methylation profiling by fluorescence melting curve analysisJ Worm, A Aggerholm, P Guldberg
Molecular and Cellular Probes|April 1, 1996
Fingerprinting sequence variation in ribosomal DNA of parasites by DGGER Gasser, P Nansen, P Guldberg
Pageof 11

Showing results (1-10 of 101) with videos related to

Sort By:
Pageof 11
Journal of Inherited Metabolic Disease|January 1, 1994
Mutation screening versus gene scanning for genotyping phenylketonuria patientsP Guldberg, F Güttler
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutations in the phenylalanine hydroxylase gene: genetic determinants for the phenotypic variability of hyperphenylalaninemiaF Güttler, P Guldberg
Nucleic Acids Research|March 11, 1994
'Broad-range' DGGE for single-step mutation scanning of entire genes: application to human phenylalanine hydroxylase geneP Guldberg, F Güttler
Nucleic Acids Research|May 11, 1993
A simple method for identification of point mutations using denaturing gradient gel electrophoresisP Guldberg, F Güttler
European Journal of Pediatrics|July 1, 1996
The influence of mutations of enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiencyF Güttler, P Guldberg
Annals of Medicine|June 1, 1992
PCR in the diagnosis of phenylketonuriaP Guldberg, F Güttler
European Journal of Pediatrics|October 24, 2000
Mutation analysis anticipates dietary requirements in phenylketonuriaF Güttler, P Guldberg
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutations in the phenylalanine hydroxylase gene: methods for their characterizationP Guldberg, F Güttler
Clinical Chemistry|June 28, 2001
In-tube DNA methylation profiling by fluorescence melting curve analysisJ Worm, A Aggerholm, P Guldberg
Molecular and Cellular Probes|April 1, 1996
Fingerprinting sequence variation in ribosomal DNA of parasites by DGGER Gasser, P Nansen, P Guldberg
Pageof 11