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

Prenatal and newborn screening for CFTR mutations: the difficulties of prediction.

Clinical biochemistry - 1 May 2011

Schwarz Martin J

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 Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to False Positive Reactions
Share to Fetus

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

Share to Neonatal Screening

Share to Predictive Value of Tests

Share to Prenatal Diagnosis

Share to Trypsin

Source

Identifiers

PMID: 22036338
DOI: 10.1016/j.clinbiochem.2011.02.018

Genes

CFTR

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal and newborn screening for CFTR mutations: the difficulties of prediction.PMID 22036338Read ↗

Rapid detection of CFTR gene rearrangements impacts on genetic counselling in cystic fibrosis.Semantic proximity Read ↗

Applying CFTR molecular genetics to facilitate the diagnosis of cystic fibrosis through screening.Semantic proximity Read ↗

Newborn screening for cystic fibrosis: the practical implications.Semantic proximity Read ↗

Prenatal prediction of cystic fibrosis in a mother homozygous for the delta F508 mutation.Semantic proximity Read ↗

Cystic fibrosis genetic counseling difficulties due to the identification of novel mutations in the CFTR gene.Semantic proximity Read ↗

Carrier screening for cystic fibrosis.Semantic proximity Read ↗

Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forward.Semantic proximity Read ↗

Prenatal screening for cystic fibrosis: where are we now?Semantic proximity Read ↗

Prenatal screening for cystic fibrosis: past, present and future.Semantic proximity Read ↗

The Impact of the CFTR Gene Discovery on Cystic Fibrosis Diagnosis, Counseling, and Preventive Therapy.Semantic proximity Read ↗

Clinical sensitivity of prenatal screening for cystic fibrosis via CFTR carrier testing in a United States panethnic populationSemantic proximity Read ↗

The Role of Extended CFTR Gene Sequencing in Newborn Screening for Cystic FibrosisSemantic proximity Read ↗

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