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

On the trail of genetic culprits in Williams syndrome.

Cardiovascular research - 1 Nov 1997

Keating M T

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 Drug Hypersensitivity
Share to Elastin
Share to Gene Deletion
Share to Infant, Newborn

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

Share to Phenotype

Share to Vitamin D

Share to Williams Syndrome

Source

Identifiers

PMID: 9463625
DOI: 10.1016/s0008-6363(97)00027-8

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

On the trail of genetic culprits in Williams syndrome.PMID 9463625Read ↗

Williams syndrome: an update on clinical and molecular aspects.Semantic proximity Read ↗

The Williams-Beuren Syndrome-a window into genetic variants leading to the development of cardiovascular disease.Semantic proximity Read ↗

Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder.Semantic proximity Read ↗

Mendelian PuzzlesSemantic proximity Read ↗

A needle in a haystack: Sturge-Weber syndrome gene discovery.Semantic proximity Read ↗

Werner syndrome: molecular genetics and mechanistic hypotheses.Semantic proximity Read ↗

Using case study comparisons to explore genotype-phenotype correlations in Williams-Beuren syndrome.Semantic proximity Read ↗

Alagille syndrome: chipping away at the tip of the iceberg.Semantic proximity Read ↗

COVID-19 and Down syndrome: the spark in the fuelSemantic proximity Read ↗

The next generation of Silver-Russell syndrome.Semantic proximity Read ↗

Genetic susceptibility to birth defects in humans: from gene discovery to public health action.Semantic proximity Read ↗

Expanding the genetic profile of Hay-Wells syndrome.Semantic proximity Read ↗

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