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

Fetal bowel hyperechogenicity may indicate mild atypical cystic fibrosis: a case associated with a complex CFTR allele.

Journal of medical genetics - 1 Aug 2000

Abramowicz M J, Dessars B, Sevens C, Goossens M, Girodon-Boulandet E

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 Child, Preschool
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to Genetic Counseling

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

Share to Heterozygote

Share to Infant, Newborn

Share to Intestines

Share to Pregnancy

Source

Open in PubMed Open full text

Identifiers

PMID: 10922395
DOI: 10.1136/jmg.37.8.e15
PMCID: PMC1734656

Genes

CFTR

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

Fetal bowel hyperechogenicity may indicate mild atypical cystic fibrosis: a case associated with a complex CFTR allele.PMID 10922395Read ↗

Cystic fibrosis screening: a fetus with hyperechogenic bowel may be the index case.Semantic proximity Read ↗

Hyperechogenic bowel loops and meconium ileus in a fetus carrying the D1152H and G542X cystic fibrosis CFTR mutations.Semantic proximity Read ↗

Predicting the risk of cystic fibrosis with abnormal ultrasound signs of fetal bowel: results of a French molecular collaborative study based on 641 prospective cases.Semantic proximity Read ↗

Comprehensive description of CFTR genotypes and ultrasound patterns in 694 cases of fetal bowel anomalies: a revised strategy.Semantic proximity Read ↗

Mid-trimester hyperechogenic bowel in a fetus of Turkish origin carrying a rarely seen mutation of cystic fibrosis.Semantic proximity Read ↗

Hyperechogenic fetal bowel: a large French collaborative study of 682 cases.Semantic proximity Read ↗

Calculating posterior cystic fibrosis risk with echogenic bowel and one characterized cystic fibrosis mutation: avoiding pitfalls in the risk calculations.Semantic proximity Read ↗

Bowel ultrasound imaging in patients with cystic fibrosis: Relationship with clinical symptoms and CFTR genotype.Semantic proximity Read ↗

Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation.Semantic proximity Read ↗

The risk of cystic fibrosis with prenatally detected echogenic bowel in an ethnically and racially diverse North American population.Semantic proximity Read ↗

Incidence of chromosomopathies and cystic fibrosis mutations in second trimester fetuses with isolated hyperechoic bowel.Semantic proximity Read ↗

Nonvisualization of fetal gallbladder increases the risk of cystic fibrosis.Semantic proximity Read ↗

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