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

[Rett syndrome: congenital defect of a transcription inhibitory protein].

Ugeskrift for laeger - 31 Jan 2000

Nielsen J B, Skovby F

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 DNA-Binding Proteins
Share to Infant
Share to Mutation
Share to Repressor Proteins

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

Share to Rett Syndrome

Share to Transcription, Genetic

Share to X Chromosome

Source

Identifiers

PMID: 10707603

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

[Rett syndrome: congenital defect of a transcription inhibitory protein].PMID 10707603Read ↗

[Rett syndrome].Semantic proximity Read ↗

[Contemporary views on Rett's syndrome: clinical, cytogenetic and molecular studies].Semantic proximity Read ↗

Introduction: Rett syndrome.Semantic proximity Read ↗

[Rett syndrome: a diagnostic, clinical and molecular update].Semantic proximity Read ↗

[Clinical features in Rett syndrome: MECP2-, CDKL5- and FOXG1- related disorders].Semantic proximity Read ↗

[Molecular basis of Rett syndrome: A current look].Semantic proximity Read ↗

Rett syndrome: recent research progress.Semantic proximity Read ↗

[Fragile X syndrome, a disease caused by defects in an RNA-binding protein].Semantic proximity Read ↗

[Rett syndrome in a child treated with adrenocorticotrophic hormone].Semantic proximity Read ↗

[Novel approaches to the background of developmental abnormalities: clinical genetics of transcription factors].Semantic proximity Read ↗

[Positional cloning of anomaly-syndrome-causing genes].Semantic proximity Read ↗

[A case of Van Wyk-Grumbach syndrome with inherited RET gene variation].Semantic proximity Read ↗

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