Cystic fibrosis and the gulf states

Qatar Medical Journal

Volumn 9, Issue 2, 2000, Pages 3-4

  Dawson, K P ^a   Al Whadneh, A ^a  

^a UNITED ARAB EMIRATES UNIVERSITY   (United Arab Emirates)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ALLELE; CYSTIC FIBROSIS; EDITORIAL; ELECTROLYTE INTAKE; FLUID INTAKE; GENE EXPRESSION; GENE FUNCTION; GENE MUTATION; GENE SEQUENCE; GENE STRUCTURE; GENETIC VARIABILITY; GENOTYPE; GEOGRAPHIC DISTRIBUTION; HUMAN; HYPOCHLOREMIA; HYPONATREMIA; INCIDENCE; LEBANON; MOLECULAR GENETICS; OMAN; PHENOTYPE; PREVALENCE; SAUDI ARABIA; SUMMER; TEMPERATURE; UNITED ARAB EMIRATES;

EID: 0034455098     PISSN: 02538253     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Editorial

References (11)

1. Cystic fibrosis
2. Cystic fibrosis in Kuwait
3. Genetic and clinical data of cystic fibrosis patients in a tertiary care centre in Saudi Arabia
4. Metabolic alkalosis in cystic fibrosis atypical presentation in Kuwait
5. Pseudo-Bartter's syndrome in an Omani infant
6. Cystic fibrosis in Lebanon: Distribution of CFTR mutations among Arab communities
7. Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation I1234V
8. Novel and characteristic CFTR mutation in Saudi Arab children with severe cystic fibrosis
9. Genotype-phenotype correlations in cystic fibrosis: Clinical severity of mutation S549R (T>G)
10. Identification of cystic fibrosis mutation in Oman
11. Mild clinical phenotype associated with R1158X/S549R (T>G) CFTR genotype