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

Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life.

Pediatrics - 1 Sept 2004

Gunther Daniel F, Eugster Erica, Zagar Anthony J, Bryant Constance G, Davenport Marsha L, Quigley Charmian A

Abstract excerpt

OBJECTIVE: To evaluate differences in phenotype and other clinical features between patients who have Turner syndrome diagnosed incidentally (on the basis of a prenatal karyotype performed for reasons unrelated to suspicion of Turner syndrome, eg, advanced maternal age) or traditionally (on the basis of either a prenatal karyotype performed for abnormal ultrasound findings or a postnatal karyotype performed for...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Bias

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Defects, Congenital

Share to Karyotyping

Share to Kidney

Share to Mosaicism

Share to Prenatal Diagnosis

Share to Turner Syndrome

Source

Identifiers

PMID: 15342833
DOI: 10.1542/peds.2003-1122-L

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life.PMID 15342833Read ↗

Turner syndrome: Evaluation of prenatal diagnosis in 19 European registriesSemantic proximity Read ↗

Turner syndrome: From birth to adulthood.Semantic proximity Read ↗

New approach to phenotypic variability and karyotype-phenotype correlation in Turner syndrome.Semantic proximity Read ↗

Turner Syndrome Genotype and Phenotype and Their Effect on Presenting Features and Timing of DiagnosisSemantic proximity Read ↗

Turner syndrome: new insights into an old disorder.Semantic proximity Read ↗

Revisiting the Neuropsychological and Clinical Profile of Mosaic Turner Syndrome With a Ring X Chromosome.Semantic proximity Read ↗

Outcome of fetuses with Turner syndrome: a 10-year congenital anomaly register based studySemantic proximity Read ↗

Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: implications for prenatal counseling and estrogen therapy at puberty.Semantic proximity Read ↗

The prevalence of turner syndrome in girls presenting with coarctation of the aorta.Semantic proximity Read ↗

Prenatal diagnosis of 45,X/46,XX mosaicism and 45,X: implications for postnatal outcome.Semantic proximity Read ↗

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

Childhood growth hormone treatment in women with Turner syndrome - benefits and adverse effects.Semantic proximity Read ↗

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