1. Boat T, Welsh MJ, Beaudet A, Cystic Fibrosis. In: Scriver C, et al., editor. The metabolic basis of inherited disease. New York: McGraw Hill;1989. pp. 2649–2860.
2. MacDonald KD, McKenzie KR, Zeitlin PL. Cystic fibrosis transmembrane regulator protein mutations: ‘class’ opportunity for novel drug innovation. Paediatr. Drugs. 2007;9(1):1–10.
3. Tsui LC, Buchwald M. Biochemical and molecular genetics of cystic fibrosis. Adv Hum Genet. 1991;20:153–266.
4. Abeliovich D, Lavon IP, Lerer I, Cohen T, Springer C, Avital A, Cutting G. Screening for five mutations detects 97 % of cystic fibrosis (cf) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population. Am J Hum Genet. 1992;51:951–6.
5. Chernick WS, Barbero GJ. Composition of tracheobronchial secretions in cystic fibrosis of the pancreas and bronchiectasis. Pediatrics. 1959;24:739–45.