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

Possible role of imprinting in the Turner phenotype.

Journal of medical genetics - 1 Nov 1994

Chu C E, Donaldson M D, Kelnar C J, Smail P J, Greene S A, Paterson W F, Connor J M

Abstract excerpt

We have attempted to investigate the role of imprinting in the phenotype of Turner's syndrome. Sixty-three patients were investigated for parental origin of the retained normal X chromosome; 43 were found to retain the maternal X (XM) and 20 the paternal (XP). The relationship between a child's p...

Topics

Female
Genomic Imprinting
Humans
Karyotyping
Male
Phenotype
Turner Syndrome
X Chromosome

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7853366
DOI: 10.1136/jmg.31.11.840
PMCID: PMC1016655

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7853366-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Possible role of imprinting in the Turner phenotype.PMID 7853366Read ↗

The physical phenotype of girls and women with Turner syndrome is not X-imprinted.Semantic proximity Read ↗

Impact of parental origin of X-chromosome on clinical and biochemical profile in Turner syndrome.Semantic proximity Read ↗

Genomic imprinting and Turner syndrome.Semantic proximity Read ↗

Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy.Semantic proximity Read ↗

Genomic imprinting in Turner syndrome: effects on response to growth hormone and on risk of sensorineural hearing loss.Semantic proximity Read ↗

The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype.Semantic proximity Read ↗

The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome.Semantic proximity Read ↗

Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome.Semantic proximity Read ↗

Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.Semantic proximity Read ↗

Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome.Semantic proximity Read ↗

Is there an influence of X-chromosomal imprinting on the phenotype in Klinefelter syndrome? A clinical and molecular genetic study of 61 cases.Semantic proximity Read ↗

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