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

Genetic Testing for Global Developmental Delay in Early Childhood

5 Jun 2024

Abstract excerpt

Importance: Global developmental delay (GDD) is characterized by a complex etiology, diverse phenotypes, and high individual heterogeneity, presenting challenges for early clinical etiologic diagnosis. Cognitive impairment is the core symptom, and despite the pivotal role of genetic factors in GDD development, the understanding of them remains limited. Objectives: To assess the utility of genetic detection in...

Read the complete abstract on PubMed

Topics

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

Share to Genomic variations and chromosomal abnormalities
Share to Genomics and Rare Diseases
Share to Neurogenetic and Muscular Disorders Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 38837156
DOI: 10.1001/jamanetworkopen.2024.15084

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic Testing for Global Developmental Delay in Early ChildhoodPMID 38837156Read ↗

Genetic testing and analysis of 1024 children with global developmental delay or intellectual disability: a single-center cohort study.Semantic proximity Read ↗

Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: a prospective studySemantic proximity Read ↗

Genetic background of idiopathic neurodevelopmental delay patients with significant brain deviation volume.Semantic proximity Read ↗

Diagnostic Utility of Trio–Exome Sequencing for Children With Neurodevelopmental DisordersSemantic proximity Read ↗

Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing.Semantic proximity Read ↗

An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure.Semantic proximity Read ↗

Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disordersSemantic proximity Read ↗

Common genetic variants contribute to risk of rare severe neurodevelopmental disordersSemantic proximity Read ↗

Genomic Diagnosis for Neurodevelopmental Disorders: Revolution, Evolution, And Current Reflections on the “Rational Diagnostic Evaluation”Semantic proximity Read ↗

Genetic and phenotypic analysis of 225 Chinese children with developmental delay and/or intellectual disability using whole-exome sequencing.Semantic proximity Read ↗

The genetic architecture of monogenic neurodevelopmental disorders in Pakistan: a systematic review, 2006–2024Semantic proximity Read ↗

Clinical use of whole exome sequencing in children with developmental delay/intellectual disabilitySemantic proximity Read ↗

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