Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Correlations between genotype and phenotype in children with phenylketonuria?].

Archives francaises de pediatrie - 1 May 1991

Labrune P, Lyonnet S

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Gene Expression Regulation, Enzymologic
Share to Genotype
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenylalanine Hydroxylase

Share to Phenylketonurias

Source

Identifiers

PMID: 1859242

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Correlations between genotype and phenotype in children with phenylketonuria?].PMID 1859242Read ↗

Relation between phenotype and genotype in phenylketonuric patients from Bulgaria.Semantic proximity Read ↗

Phenotype distribution in the Spanish phenylketonuria population and related genotypes.Semantic proximity Read ↗

Phenylketonuria - genetic, clinical and therapeutic aspectsSemantic proximity Read ↗

[Molecular genetics of phenylketonuria in Novosibirsk Region].Semantic proximity Read ↗

Pathogenesis of different clinical outcomes in spite of identical genotypes and comparable blood phenylalanine concentrations in phenylketonurics.Semantic proximity Read ↗

Relation between phenylalanine hydroxylase genotypes and phenotypic parameters of diagnosis and treatment of hyperphenylalaninaemic disorders. German Collaborative Study of PKU.Semantic proximity Read ↗

Different phenotypic manifestations associated with identical phenylketonuria genotypes in two Spanish families.Semantic proximity Read ↗

Heterogeneity of phenylketonuria in Belgium at the genotype-phenotype level.Semantic proximity Read ↗

Molecular genetics of phenylketonuria: from molecular anthropology to gene therapy.Semantic proximity Read ↗

[Phenotype--genotype relationships in peroxisome biogenesis disorders].Semantic proximity Read ↗

[Correlation between genotypes and biochemical phenotypes of phenylalanine hydroxylase in patients with phenylketonuria].Semantic proximity Read ↗

Phenylketonuria in Portugal: Genotype-phenotype correlations using molecular, biochemical, and haplotypic analyses.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.