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

Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services

2 Nov 2013

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Autism Spectrum Disorder Research
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 24188901
DOI: 10.1016/j.gene.2013.10.020

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic servicesPMID 24188901Read ↗

Chromosomal microarray analyses from 5,778 patients with neurodevelopmental disorders and congenital anomalies in BrazilSemantic proximity Read ↗

The impact of chromosomal microarray on clinical management: a retrospective analysis.Semantic proximity Read ↗

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental DisordersSemantic proximity Read ↗

Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital AnomaliesSemantic proximity Read ↗

Chromosomal Microarray in Patients with Non-Syndromic Autism Spectrum Disorders in the Clinical Routine of a Tertiary HospitalSemantic proximity Read ↗

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital AnomaliesSemantic proximity Read ↗

Clinical Utility of Chromosomal Microarray AnalysisSemantic proximity Read ↗

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomaliesSemantic proximity Read ↗

Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in BrazilSemantic proximity Read ↗

The utility of chromosomal microarray analysis in developmental and behavioral pediatrics.Semantic proximity Read ↗

Chromosomal Microarray versus Karyotyping for Prenatal DiagnosisSemantic proximity Read ↗

Dual testing strategy in autism increases diagnostic yield: Chromosomal microarray and whole-exome sequencing combination may be best for children with multiple physical anomalies, study suggests.Semantic proximity Read ↗

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