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Article

Multiple mutation analysis of the cystic fibrosis gene in single cells.

Molecular human reproduction - 1 Jun 2005

Sánchez-García Jorge Fernando, Benet Jordi, Gutiérrez-Mateo Cristina, Luís Séculi José, Monrós Eugènia, Navarro Joaquima

Abstract excerpt

PGD is becoming an alternative to prenatal diagnosis. The combination of IVF techniques with the PCR technology allows for the detection of genetic abnormalities in first polar bodies from oocytes and blastomeres from cleavage-stage embryos. Dealing with a genetic disease with a heterogeneous spectrum of mutations like cystic fibrosis, one of the objectives of centres offering PGD is the application of simple and...

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

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Source

Identifiers

PMID: 15908456
DOI: 10.1093/molehr/gah176

Genes

PGD
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.

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Multiple mutation analysis of the cystic fibrosis gene in single cells.PMID 15908456Read ↗

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