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

Non-syndromic X linked intellectual disability: Current knowledge in light of the recent advances in molecular and functional studies.

Clinical genetics - 1 May 2020

Tejada María Isabel, Ibarluzea Nekane

Abstract excerpt

Since the discovery of the FMR1 gene and the clinical and molecular characterization of Fragile X Syndrome in 1991, more than 141 genes have been identified in the X-chromosome in these 28 years thanks to applying continuously evolving molecular techniques to X-linked intellectual disability (XLID) families. In the past decade, array comparative genomic hybridization and next generation sequencing technologies...

Read the complete abstract on PubMed

Topics

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

Share to Comparative Genomic Hybridization
Share to Fragile X Mental Retardation Protein

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

Share to Fragile X Syndrome

Share to Genes, X-Linked

Share to Genetic Diseases, X-Linked

Share to High-Throughput Nucleotide Sequencing

Share to Intellectual Disability

Share to X-Linked Intellectual Disability

Source

Identifiers

PMID: 31898314
DOI: 10.1111/cge.13698

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

Non-syndromic X linked intellectual disability: Current knowledge in light of the recent advances in molecular and functional studies.PMID 31898314Read ↗

Fragile X and X-linked intellectual disability: four decades of discovery.Semantic proximity Read ↗

Four families with X-linked intellectual disability affected males: Novel deleterious variants and clinical features with the review of literatureSemantic proximity Read ↗

Clinical and molecular contributions to the understanding of X-linked mental retardation.Semantic proximity Read ↗

Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature.Semantic proximity Read ↗

[X-linked mental retardation].Semantic proximity Read ↗

X-linked mental retardation: many genes for a complex disorder.Semantic proximity Read ↗

The fragile-X syndrome: a growing gene causing familial intellectual disability.Semantic proximity Read ↗

Fragile X syndrome: a review of clinical and molecular diagnoses.Semantic proximity Read ↗

The neurobiology of X-linked intellectual disability.Semantic proximity Read ↗

X-linked mental retardation: further lumping, splitting and emerging phenotypes.Semantic proximity Read ↗

X-Linked intellectual disability update 2022.Semantic proximity Read ↗

X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms.Semantic proximity Read ↗

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