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Article

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

Journal of medical genetics - 1 May 2004

Ogino S, Wilson R B, Grody W W

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Share to Bayes Theorem
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to Genes, Recessive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, Inborn

Share to Intestines

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Share to Ultrasonography, Prenatal

Source

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Identifiers

PMID: 15121798
DOI: 10.1136/jmg.2003.015065
PMCID: PMC1735756

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation.PMID 15121798Read ↗

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Conveying a probabilistic genetic test result to families with an inherited heart diseaseSemantic proximity Read ↗

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

Bayesian analysis and risk assessment in genetic counseling and testing.Semantic proximity Read ↗

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

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