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

Monogenic and chromosomal causes of isolated speech and language impairment.

Journal of medical genetics - 1 Nov 2015

Barnett C P, van Bon B W M

Abstract excerpt

The importance of a precise molecular diagnosis for children with intellectual disability, autism spectrum disorder and epilepsy has become widely accepted and genetic testing is an integral part of the diagnostic evaluation of these children. In contrast, children with an isolated speech or language disorder are not often genetically evaluated, despite recent evidence supporting a role for genetic factors in the...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Disorders

Share to Disease Management

Share to DNA Copy Number Variations

Share to Language Development Disorders

Share to Speech Disorders

Source

Identifiers

PMID: 26139234
DOI: 10.1136/jmedgenet-2015-103161

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Monogenic and chromosomal causes of isolated speech and language impairment.PMID 26139234Read ↗

The clinical and genetic spectrum of paediatric speech and language disorders.Semantic proximity Read ↗

Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.Semantic proximity Read ↗

Genetic advances in the study of speech and language disorders.Semantic proximity Read ↗

The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individualsSemantic proximity Read ↗

Childhood motor speech disorders: who to prioritise for genetic testingSemantic proximity Read ↗

Genetics, Syndromes, and Communication DisordersSemantic proximity Read ↗

Consensus recommendations on communication, language and speech in Phelan-McDermid syndrome.Semantic proximity Read ↗

[Genetic causes in mild speech acquisition delay with/without mild developmental delay: significance for ENT physicians].Semantic proximity Read ↗

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developmentSemantic proximity Read ↗

Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature.Semantic proximity Read ↗

Genetics of Cerebral Palsy: Diagnosis, Differential Diagnosis, and BeyondSemantic proximity Read ↗

Developmental trajectories in 22q11.2 deletion syndromeSemantic proximity Read ↗

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