Viviane Dumur

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

Mireille Claustres, Caroline Guittard, Dominique Bozon et al. · Human Mutation · 2000 · 250 citations

The sialylation of bronchial mucins secreted by patients suffering from cystic fibrosis or from chronic bronchitis is related to the severity of airway infection

M Davril, Sophie Groux‐Degroote, P. Humbert et al. · Glycobiology · 1999 · 121 citations · Full text

Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype

Viviane Dumur, Radj Gervais, Jean‐Marc Rigot et al. · Human Genetics · 1996 · 91 citations

Developmental Biology, Genetics, Pathology +3

CFTR genotypes in patients with normal or borderline sweat chloride levels

Delphine Feldmann, Rémy Couderc, Marie‐Pierre Audrézet et al. · Human Mutation · 2003 · 71 citations

Molecular Diagnostic Techniques, Mendelian Disorder, Genetic Disorder +11

Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy

Dominique Marchant, Karı̈n Gogat, Sandrine Boutboul et al. · Human Mutation · 2001 · 52 citations · Full text