Author:
Braekeleer M.,Allard C.,Leblanc J. -P.,Aubin G.,Simard F.
Publisher
Springer Science and Business Media LLC
Subject
Infectious Diseases,Microbiology (medical),General Medicine
Reference15 articles.
1. Boat TF, Welsh MJ, Beaudet AL: Cystic fibrosis. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds): The metabolic basis of inherited disease. McGraw-Hill, New York (1989) pp. 2649–2680.
2. Daigneault J, Aubin G, Simard F, De Braekeleer M: Genetic epidemiology of cystic fibrosis in Saguenay-Lac-St-Jean (Québec, Canada). Clinical Genetics (1991) 40:298–303.
3. Rozen R, De Braekeleer M, Daigneault J, Ferreira-Rajabi L, Gerdes M, Lamoureux L, Aubin G, Simard F, Fujiwara TM, Morgan K: Cystic fibrosis mutations in French Canadians: three mutations are relatively frequent in a Québec population which has an elevated incidence of cystic fibrosis. American Journal of Medical Genetics (1992) 42:360–364.
4. Kerem E, Corey M, Gold R, Levison H: Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization withPseudomonas aeruginosa. Journal of Pediatrics (1990) 116:714–719.
5. Hudson VL, Wielinski CL, Regelmann WE: Prognostic implications of initial oropharyngeal bacterial flora in patients with cystic fibrosis diagnosed before the age of two years. Journal of Pediatrics (1993) 122:854–860.