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Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTRmutation
- Dr Dalton,molecular.gen{at}sheffield.ac.uk
Citation
Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTRmutation
Publication history
- First published July 1, 2000.
Online issue publication
April 27, 2016
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Journal of Medical Genetics