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Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.
- Published in:
- Human Genetics, 2000, v. 106, n. 3, p. 259, doi. 10.1007/s004390000246
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- Article