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The cloning of the gene that is defective in cystic fibrosis (CF) has provided a means for accurate genetic diagnosis, defining the basic cellular defect, and developing new treatment strategies.
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Key Phrases - Statistically Improbable Phrases (SIPs):
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conventional chest physiotherapy, mist tent therapy, overt right heart failure, mucin peptide core, bronchiectatic cysts, chronic pseudomonas infection, reabsorptive duct, amiloride aerosol, secretory clearance, chronic endobronchial infection, distal intestinal obstruction syndrome, multilobular biliary cirrhosis, focal biliary cirrhosis, opsonized pseudomonas, cepacia colonization, pulmonary exacerbations, ductal segments, pancreatic duct cells, aeruginosa mucoid exopolysaccharide, basolateral cell membrane, pulmonary deterioration, mucin granules, mucus stasis, porcine submaxillary mucin, respiratory exacerbations
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New Engl, New York, Acta Paediatr, San Francisco, United States, Allergy Clin, Chest Med, Acta Pathol, Cell Biol, Raven Press, Agents Chemother, American Physiological Society, Liver Physiol, Marcel Dekker, The Gastrointestinal System, Academic Press, Johns Hopkins Med, Membrane Biol, Drug Intell, Elastic van Gieson, Hedman Cefsulodin, Hedman Ceftazidime, Pergamon Press, Van Asperen
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