Mireille Vibert

WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal period

Mylène Valduga, Christophe Philippe, Laëtitia Lambert et al. · Journal of Human Genetics · 2015 · 37 citations · Full text

Pediatrics, Neurology, Neuropathology +4

Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene

Céline Bonnet, M. J. Grégoire, Mireille Vibert et al. · Journal of Human Genetics · 2008 · 19 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +10

Prenatal exclusion of X‐linked hydrocephalus‐stenosis of the aqueduct of sylvius sequence using closely linked DNA markers

F Serville, Paule Bénit, Pascale Saugier-Véber et al. · Prenatal Diagnosis · 1993 · 15 citations