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Article

New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society - 1 Nov 2008

Bustamante-Aragones Ana, Gallego-Merlo Jesus, Trujillo-Tiebas Maria Jose, de Alba Marta Rodriguez, Gonzalez-Gonzalez Cristina, Glover Guillermo, Diego-Alvarez Dan, Ayuso Carmen, Ramos Carmen

Abstract excerpt

BACKGROUND: Since the presence of fetal DNA was discovered in maternal blood, different investigations have focused on non-invasive prenatal diagnosis. The analysis of fetal DNA in maternal plasma may allow the diagnosis of fetuses at risk of cystic fibrosis (CF) without any risk of fetal loss. Here, we present a new strategy for the detection of fetal mutations causing CF in maternal plasma. METHODS: We have...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 18573697
DOI: 10.1016/j.jcf.2008.05.006

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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.

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