O. Pascaud

Strategy linking several analytical methods of neonatal screening for sickle cell disease

J. Elion, R. Ducrocq, M. Benkerrou, 2001, Journal of medical screening.

Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease.

E. Denamur, A. Laquérriere, H. Le Nagard, 2010, Kidney international.

Compound heterozygosity for ΔF508 and F508C: A cautionary note on the molecular diagnosis of cystic fibrosis

E. Denamur, J. Oury, J. Elion, 1994 .

Molecular Basis of β‐Thalassemia in Bahrain: An Epicenter for a Middle East Specific Mutation a

D. Labie, J. Elion, T. Merghoub, 1998 .

Molecular basis of beta-thalassemia in Bahrain: an epicenter for a Middle East specific mutation.

D. Labie, J. Elion, T. Merghoub, 1998, Annals of the New York Academy of Sciences.

Distribution of CFTR Mutations in Cystic Fibrosis Patients of Tunisian Origin: Identification of Two Novel Mutations

E. Denamur, C. Férec, J. Elion, 1996, European journal of human genetics : EJHG.

Genotype-phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease.

E. Denamur, A. Laquérriere, M. Gonzalès, 2010, Kidney international.

Novel mutation (A141D) in exon 4 of the CFTR gene identified in an Algerian patient

E. Denamur, L. Gouya, J. Elion, 1997, Human mutation.