Related Experiment Videos
Molecular heterogeneity of nonphenylketonuria hyperphenylalaninemia in 25 Danish patients
P Guldberg1, K F Henriksen, B Thöny
1Danish Center for Human Genome Research, John F. Kennedy Institute, Glostrup.
Genomics
|May 15, 1994
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
European guidelines on diagnosis and treatment of phenylketonuria: First revision.
Molecular genetics and metabolism·2025
Forensic postmortem computed tomography in suspected unnatural adult deaths.
European journal of radiology·2020
Homocarnosinosis: A historical update and findings in the SPG11 gene.
Acta neurologica Scandinavica·2018
The complete European guidelines on phenylketonuria: diagnosis and treatment.
Orphanet journal of rare diseases·2017
Cysteamine revisited: repair of arginine to cysteine mutations.
Journal of inherited metabolic disease·2017
The challenges of managing coexistent disorders with phenylketonuria: 30 cases.
Molecular genetics and metabolism·2015
Analysis of distribution of IL13 and ADAM33 gene haplotypes in Russians, Khakass, Tuvans in relation to the risk of developing bronchial asthma.
Vavilovskii zhurnal genetiki i selektsii·2026
Analysis of leg bone lengths from whole-body dual-energy X-ray absorptiometry in the UK biobank.
BJR artificial intelligence·2026
[Congenital anosmia : a practical diagnostic approach].
Revue medicale suisse·2026