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

Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2).

American journal of medical genetics - 28 Mar 1998

Smith A C, Dykens E, Greenberg F

Abstract excerpt

Smith-Magenis syndrome (SMS) is a distinct and clinically recognizable multiple congenital anomaly (MCA) and mental retardation syndrome caused by an interstitial deletion of chromosome 17 p11.2. The phenotype of SMS has been well described and includes: a characteristic pattern of physical featu...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Child
Share to Chromosomes, Human, Pair 17

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Deletion

Share to Intellectual Disability

Share to Phenotype

Share to Syndrome

Source

Identifiers

PMID: 9613859
DOI: 10.1002/(sici)1096-8628(19980328)81:2<179::aid-ajmg10>3.0.co;2-e

Genes

SMS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-9613859-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2).PMID 9613859Read ↗

Smith-Magenis syndrome: Clinical and behavioral characteristics in a large retrospective cohort.Semantic proximity Read ↗

Cognitive and adaptive behavior profiles in Smith-Magenis syndrome.Semantic proximity Read ↗

[Smith-Magenis syndrome: a report of two new cases and an approximation to their characteristic behavioural phenotype].Semantic proximity Read ↗

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)Semantic proximity Read ↗

A case report of monozygotic twins with Smith-Magenis syndrome.Semantic proximity Read ↗

A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome.Semantic proximity Read ↗

[Smith-Magenis syndrome: case report and review].Semantic proximity Read ↗

Smith-Magenis Syndrome—Clinical Review, Biological Background and Related DisordersSemantic proximity Read ↗

Communicative competence and behavioural phenotype in children with Smith-Magenis syndrome.Semantic proximity Read ↗

Behavioral phenotype and neuropsychological profile of an adult with Smith-Magenis Syndrome due to a previously unreported RAI1 mutation: A case reportSemantic proximity Read ↗

Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases.Semantic proximity Read ↗

[Diagnostic difficulties in Smith-Magenis Syndrome (SMS) on the basis of own experience and literature data].Semantic proximity Read ↗

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