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References from Phenotypic and genetic characteristics of children with developmental delay or intellectual disability: a cohort from Northwest China. Local targets link to admitted publications; unresolved targets remain external evidence.
Developmental disabilities among children younger than 5 years in 195 countries and territories, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016
10.1016/s2214-109x(18)30309-7 · 2018 · External reference
Cerebral palsy and developmental intellectual disability in children younger than 5 years: Findings from the GBD-WHO Rehabilitation Database 2019
10.3389/fpubh.2022.894546 · 2022 · External reference
Screening, Diagnosis, and Investigation of Global Developmental Delay and Intellectual Developmental Disorder
2025 · External reference
Comprehensive evaluation of the child with global developmental delays or intellectual disability
10.3345/cep.2023.01697 · 2024 · External reference
Genetic determinants of global developmental delay and intellectual disability in Ukrainian children
10.1186/s11689-024-09528-x · 2024 · External reference
Effectiveness of Early Intervention Programs for Young Children with Global Developmental Delay: A Systematic Review
10.31661/gmj.vi.3906 · 2025 · External reference
Evaluation of Individuals with Non-Syndromic Global Developmental Delay and Intellectual Disability
2023 · External reference
Genome-Wide Sequencing Modalities for Children with Unexplained Global Developmental Delay and Intellectual Disabilities—A Narrative Review
10.3390/children10030501 · 2023 · External reference
The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing
10.1002/epi4.12719 · 2023 · External reference
10.1002/pd.4782
10.1002/pd.4782 · External reference
Chromosome microarray analysis combined with karyotype analysis is a powerful tool for the detection in pregnant women with high-risk indicators
10.1186/s12884-023-06052-z · 2023 · External reference
Global developmental delay and intellectual disability in the era of genomics: Diagnosis and challenges in resource limited areas
10.1016/j.clineuro.2023.107799 · 2023 · External reference
Genetic aetiology of global developmental delay and intellectual disability in Africa: a scoping review
10.3389/fgene.2026.1718279 · 2026 · External reference
Clinically relevant variants detected in Chinese children with global developmental delay/intellectual disability: An exome-wide sequencing study
10.1016/j.gendis.2024.101389 · 2025 · External reference
Genetic Counselling for Global Developmental Delay/Intellectual Disability (GDD/ID) - Changing Landscapes and Persisting Challenges
10.1007/s13312-023-2813-1 · 2023 · External reference
A Review of the Genomic Analysis of Children Presenting with Developmental Delay/Intellectual Disability and Associated Dysmorphic Features
2019 · External reference
Clinical and genetic profile of children with unexplained intellectual disability/developmental delay and epilepsy
10.1016/j.eplepsyres.2021.106782 · 2021 · External reference
10.1093/pch/pxy093
10.1093/pch/pxy093 · External reference
Systematic review of MRI findings in children with developmental delay or cognitive impairment
10.1016/j.braindev.2017.04.006 · 2017 · External reference
The role of chromosomal microarray and exome sequencing in prenatal diagnosis
10.1097/gco.0000000000000692 · 2021 · External reference
Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual Disability
10.1080/15513815.2020.1791292 · 2022 · External reference
Diagnostic approach with genetic tests for global developmental delay and/or intellectual disability: Single tertiary center experience
10.1111/ahg.12294 · 2019 · External reference
Targeted Next-Generation Sequencing of Korean Patients With Developmental Delay and/or Intellectual Disability
10.3389/fped.2018.00391 · 2018 · External reference
Etiological Evaluation of Global Developmental Delay
10.1007/s12098-019-03077-1 · 2020 · External reference
Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review
10.1210/clinem/dgad312 · 2023 · External reference
Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome)
10.1002/pd.6340 · 2023 · External reference
Genetic and metabolic profiling of individuals with Phelan-McDermid syndrome presenting with seizures
10.1111/cge.14074 · 2022 · External reference
Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability
10.3345/kjp.2019.00808 · 2020 · External reference
Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disability
10.1016/j.eplepsyres.2021.106552 · 2021 · External reference
Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness
10.1186/s12920-022-01287-9 · 2022 · External reference
Bioinformatics Analysis Revealed Novel 3’UTR Variants Associated with Intellectual Disability
10.3390/genes11090998 · 2020 · External reference
10.64898/2025.12.29.696848
10.64898/2025.12.29.696848 · External reference
