M.-O. Cabanis

Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database

Érick Denamur, Isabelle Henry, M.-O. Cabanis et al. · The American Journal of Human Genetics · 1998 · 232 citations · Full text

Scleroderma, Genetic Disorder, Medicine +15

6q1 monosomy: a distinctive syndrome

C Turleau, Gérard Demay, M.-O. Cabanis et al. · Clinical Genetics · 1988 · 63 citations

WT1 splicing alterations in Wilms' tumors.

David Baudry, Michel Hamelin, M.-O. Cabanis et al. · PubMed · 2000 · 31 citations

Somatic Variant, Wt1 Gene, Tumor Heterogeneity +12

[Interstitial deletion in the long arm of chromosome 7].

P. Sardá, C Turleau, M.-O. Cabanis et al. · PubMed · 1988 · 14 citations