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Genes in the vicinity of CFTR modulate the cystic fibrosis phenotype in highly concordant or discordant F508del homozygous sib pairs.
- Published in:
- Human Genetics, 2003, v. 112, n. 1, p. 1, doi. 10.1007/s00439-002-0839-7
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- Article
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
Analysis of microsatellites by direct blotting electrophoresis and chemiluminescence detection.
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- Electrophoresis, 1995, v. 16, n. 1, p. 1886, doi. 10.1002/elps.11501601309
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- Article
Genes, Environment, Ion Transport, and Cystic Fibrosis.
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- American Journal of Respiratory & Critical Care Medicine, 2004, v. 169, n. 6, p. 770, doi. 10.1164/ajrccm.169.6.950
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- Article
Cystic Fibrosis and NOS3.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2004, v. 169, n. 2, p. 319, doi. 10.1164/ajrccm.169.2.957
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- Article