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British Journal of Haematology|August 20, 2014
Next-generation sequencing is a credible strategy for blood group genotypingYann Fichou, Marie-Pierre Audrézet, Paul Guéguen, et al.
Journal of Medical Screening|April 30, 2017
Optimization of the French cystic fibrosis newborn screening programme by a centralized tracking processAnne Munck, Dominique Delmas, Marie-Pierre Audrézet, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 11, 2007
Estimating the age of CFTR mutations predominantly found in Brittany (Western France)Yann Fichou, Emmanuelle Génin, Cédric Le Maréchal, et al.
Human Mutation|September 30, 2014
Genetics and pathogenesis of autosomal dominant polycystic kidney disease: 20 years onEmilie Cornec-Le Gall, Marie-Pierre Audrézet, Yannick Le Meur, et al.
Orphanet Journal of Rare Diseases|March 3, 2012
Evidence for decline in the incidence of cystic fibrosis: a 35-year observational study in Brittany, FranceVirginie Scotet, Ingrid Duguépéroux, Philippe Saliou, et al.
The Journal of Pediatrics|December 25, 2007
Time trends in birth incidence of cystic fibrosis in two European areas: data from newborn screening programsVirginie Scotet, Baroukh M Assael, Ingrid Duguépéroux, et al.
Human Genetics|May 28, 2003
Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, FranceVirginie Scotet, Marie-Pierre Audrézet, Michel Roussey, et al.
American Journal of Obstetrics and Gynecology|October 12, 2010
Focus on cystic fibrosis and other disorders evidenced in fetuses with sonographic finding of echogenic bowel: 16-year report from Brittany, FranceVirginie Scotet, Ingrid Duguépéroux, Marie-Pierre Audrézet, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 1, 2013
Cascade testing in families of carriers identified through newborn screening in Western Brittany (France)Ingrid Duguépéroux, Marie-Pierre Audrézet, Philippe Parent, et al.
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