METHOD OF DETECTING CYSTIC FIBROSIS ASSOCIATED MUTATIONS

The present invention describes a method for the simultaneous identification of two or more single base changes, insertions, deletions or translocations in a plurality of target nucleotide sequences that are markers associated with cystic fibrosis. Multiplex detection is accomplished using multiplex...

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Hauptverfasser: GALVAN, BARBARA, LISLE, CONNIE
Format: Patent
Sprache:eng ; fre
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