Prenatal diagnosis of cystic fibrosis by multiplex PCR of mutation and microsatellite alleles
- 17 August 1991
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 338 (8764), 458
- https://doi.org/10.1016/0140-6736(91)91092-9
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- CAGT Microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingoverGenomics, 1991
- A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator proteinNature, 1990
- Δ F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish familiesPrenatal Diagnosis, 1990
- Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patientsCell, 1990
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989