Abnormal frequency of delta F508 mutation in neonatal transitory hypertrypsinaemia
- PMID: 1670678
- DOI: 10.1016/0140-6736(91)93377-l
Abnormal frequency of delta F508 mutation in neonatal transitory hypertrypsinaemia
Comment on
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Abnormal distribution of cystic fibrosis delta F508 allele in adults with chronic bronchial hypersecretion.Lancet. 1990 Jun 2;335(8701):1340. doi: 10.1016/0140-6736(90)91216-w. Lancet. 1990. PMID: 1971393 No abstract available.
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