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

Visual-Motor Integration Deficits in 3q29 Deletion Syndrome.

Journal of autism and developmental disorders - 1 Aug 2024

Pollak Rebecca M, Burrell T Lindsey, Cubells Joseph F, Klaiman Cheryl, Murphy Melissa M, Saulnier Celine A, Walker Elaine F, White Stormi Pulver, Mulle Jennifer G

Abstract excerpt

3q29 deletion syndrome (3q29del) is associated with neuropsychiatric and neurodevelopmental phenotypes. We previously reported that graphomotor weakness is present in up to 78% of individuals with 3q29del. We have now explored nuances of the graphomotor phenotype and its association with other comorbidities in this population. Participants were recruited from the online 3q29 registry (3q29deletion.org) for two...

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 Chromosome Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 3

Share to Developmental Disabilities

Share to Executive Function

Share to Intellectual Disability

Share to Psychomotor Performance

Share to Visual Perception

Source

Open in PubMed Open full text

Identifiers

PMID: 37354284
DOI: 10.1007/s10803-023-06034-2
PMCID: PMC11300491

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

Visual-Motor Integration Deficits in 3q29 Deletion Syndrome.PMID 37354284Read ↗

Visual-motor integration deficits in 3q29 deletion syndromeSemantic proximity Read ↗

Comprehensive phenotyping of 3q29 deletion syndrome: recommendations for clinical careSemantic proximity Read ↗

Adaptive behavior deficits in individuals with 3q29 deletion syndromeSemantic proximity Read ↗

Systematic Description of 3q29 Duplication Syndrome Reveals New Syndromic Phenotypes: Results from the 3q29 RegistrySemantic proximity Read ↗

3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients.Semantic proximity Read ↗

MED13L-related disorder characterized by severe motor speech impairmentSemantic proximity Read ↗

Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report.Semantic proximity Read ↗

Beyond IQ: Executive function deficits and their relation to functional, clinical, and neuroimaging outcomes in 3q29 deletion syndromeSemantic proximity Read ↗

Musculoskeletal phenotypes in 3q29 deletion syndromeSemantic proximity Read ↗

Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome.Semantic proximity Read ↗

Musculoskeletal phenotypes in 3q29 deletion syndrome.Semantic proximity Read ↗

New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry.Semantic proximity Read ↗

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