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

Facial features in children with the 22q11 deletion syndrome.

Acta paediatrica (Oslo, Norway : 1992) - 1 Aug 2008

Oskarsdóttir S, Holmberg E, Fasth A, Strömland K

Abstract excerpt

AIM: To find a pattern of the most typical facial features in children with the 22q11 deletion syndrome, which could serve as an aid in identifying patients with the syndrome. METHODS: In 80 children and adolescents with the 22q11 deletion syndrome, three investigators evaluated the facial featur...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 22
Share to Ear, External

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Facial Expression

Share to Infant

Source

Identifiers

PMID: 18482168
DOI: 10.1111/j.1651-2227.2008.00858.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-18482168-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Facial features in children with the 22q11 deletion syndrome.PMID 18482168Read ↗

The facial phenotype of the velo-cardio-facial syndrome.Semantic proximity Read ↗

Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey.Semantic proximity Read ↗

22q11.2 deletion syndrome in diverse populations.Semantic proximity Read ↗

Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.Semantic proximity Read ↗

Nablus mask-like facial syndrome: Report of an atypical case with 8q21.3-q22.1 deletion.Semantic proximity Read ↗

Phenotype of adults with the 22q11 deletion syndrome: A review.Semantic proximity Read ↗

Objective studies of the face of Noonan, Cardio-facio-cutaneous, and Costello syndromes: A comparison of three disorders of the Ras/MAPK signaling pathway.Semantic proximity Read ↗

Williams-Beuren syndrome in diverse populations.Semantic proximity Read ↗

Presenting phenotype in 100 children with the 22q11 deletion syndrome.Semantic proximity Read ↗

Craniofacial phenotypes associated with Robinow syndrome.Semantic proximity Read ↗

A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome.Semantic proximity Read ↗

[22q11 deletion syndrome: an expanding phenotype].Semantic proximity Read ↗

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