DNA Analysis in CF Families by Biotinylated Probes and Polymerase Chain Reaction Technique
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 290)
About 70% of the mutations in the cystic fibrosis (CF) gene in North American, British and Dutch patients are caused by a 3 bp deletion referred to as DeltaF508 (Kerem et al., 1989).
KeywordsCystic Fibrosis Prenatal Diagnosis Polymerase Chain Reaction Technique Informative Pattern Carrier Detection
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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- Mathew, C.G. ,Roberts, R.G., Harris, A., Bentley, D.P., Bobrow, M., 1989, Rapid screening for DeltaF508 deletion in Cystic Fibrosis, Lancet, II:1346.Google Scholar
© Springer Science+Business Media New York 1991