Genetic determinants ofPseudomonas aeruginosacolonization in cystic fibrosis patients in Canada
โ Scribed by M. De Braekeleer; C. Allard; J. -P. Leblanc; G. Aubin; F. Simard
- Publisher
- Springer
- Year
- 1998
- Tongue
- English
- Weight
- 311 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0934-9723
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
To determine the number and frequency of mutations that occur at the cystic fibrosis locus (CF), we have examined the allele and haplotype frequencies of eight polymorphic DNA markers linked to CF in 163 Italian patients who were sub-divided according to their clinical presentations. The distributio
Poor nutritional status in patients with cystic fibrosis (CF) is associated with increased mortality. Patients with CF often have a decreased sensation of smell secondary to recurrent sinus infections or sinus surgery; in other CF populations, a decreased sensation of smell has been associated with
## for the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis Summary. Cystic fibrosis (CF) is a complex illness characterized by chronic lung infection leading to deterioration in function and respiratory failure in over 85% of patients. An understanding of the risk fact
## Communicuted by Garry R. Cutting Cystic fibrosis is the most common autosomal recessive disorder in Caucasian populations, with an approximate frequency of 112500 live births and a carrier frequency of 1125. Due to the high rate of predicted carriers (>63,000) in the Nebraska population (1990 U