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

Molecular analysis of PKU haplotypes in the population of southern Poland.

Human genetics - 1 Jan 1991

Zygulska M, Eigel A, Aulehla-Scholz C, Pietrzyk J J, Horst J

Abstract excerpt

Out of a population of 138,598 infants born in southern Poland between 1987 and 1989, and screened for phenylketonuria (PKU), 28 cases were ascertained probands and their parents were isolated and eight polymorphic restriction sites were analyzed within the phenylalanine hydroxylase gene region....

Topics

Alleles
DNA
DNA Restriction Enzymes
Europe
Haplotypes
Humans
Incidence
Leukocytes
Phenylketonurias
Poland
Polymorphism, Restriction Fragment Length

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1671770
DOI: 10.1007/BF00202412

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-1671770-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular analysis of PKU haplotypes in the population of southern Poland.PMID 1671770Read ↗

Phenylketonuria in Poland: 66% of PKU alleles are caused by three mutations.Semantic proximity Read ↗

Mutation spectrum and phenylalanine hydroxylase RFLP/VNTR background in 44 Romanian phenylketonuric alleles.Semantic proximity Read ↗

Mutation and haplotype analysis of phenylalanine hydroxylase alleles in classical PKU patients from the Czech Republic: identification of four novel mutations.Semantic proximity Read ↗

The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria.Semantic proximity Read ↗

Haplotype distribution at the phenylalanine hydroxylase locus in PKU families from the Moravian area of Czechoslovakia.Semantic proximity Read ↗

Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy.Semantic proximity Read ↗

PKU in Slovakia: mutation screening and haplotype analysis.Semantic proximity Read ↗

Phenylketonuria mutations and their relation to RFLP haplotypes at the PAH locus in Czech PKU families.Semantic proximity Read ↗

[Molecular genetic aspects of phenylketonuria (PKU)].Semantic proximity Read ↗

Haplotype distribution and molecular defects of PKU in Italy.Semantic proximity Read ↗

Molecular characterization of PKU allele prevalent in southern Europe and Ireland.Semantic proximity Read ↗

Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families.Semantic proximity Read ↗

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