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Article

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

Prenatal diagnosis - 1 Jul 2002

Orgad Shlomit, Berkenstadt Michal, Achiron Reuven, Yahav Yaakov, Gazit Ephraim, Barkai Gad, Loewenthal Ron

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Share to Amniotic Fluid
Share to Cystic Fibrosis Transmembrane Conductance Regulator
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12124706
DOI: 10.1002/pd.362

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.

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Hyperechogenic bowel loops and meconium ileus in a fetus carrying the D1152H and G542X cystic fibrosis CFTR mutations.PMID 12124706Read ↗

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

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

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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 ↗

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A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene.Semantic proximity Read ↗

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

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