[Congenital chromosomal syndromes-model of pathogenicity].

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

Community

Back to search

Article

[Congenital chromosomal syndromes-model of pathogenicity].

Postepy higieny i medycyny doswiadczalnej - 1 Jan 2000

Hübner H, Magnuski J

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 Autoantibodies
Share to Chromosome Aberrations
Share to Chromosome Disorders
Share to Klinefelter Syndrome

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Metabolism, Inborn Errors

Share to Models, Biological

Share to Sex Chromosome Aberrations

Share to Turner Syndrome

Source

Open in PubMed

Identifiers

PMID: 4884761

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Congenital chromosomal syndromes-model of pathogenicity].PMID 4884761Read ↗

[New chromosomal syndromes].Semantic proximity Read ↗

[Congenital Horner's syndrome].Semantic proximity Read ↗

[William's syndrome: from phenotype to genotype].Semantic proximity Read ↗

[William's syndrome: a phenotypic diagnosis].Semantic proximity Read ↗

[Molecular genetic understanding of hereditary disorders].Semantic proximity Read ↗

[Dilemma of inherited cat diseases].Semantic proximity Read ↗

[Interstitial lung disease in infants caused by genetic abnormalities].Semantic proximity Read ↗

[Fragile X syndrome].Semantic proximity Read ↗

[Prospects for genetic diagnosis].Semantic proximity Read ↗

[Positional cloning of anomaly-syndrome-causing genes].Semantic proximity Read ↗

[Mosaic trisomy 13].Semantic proximity Read ↗

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