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List of works by Solenn Pruvost

A new TRPV3 missense mutation in a patient with Olmsted syndrome and erythromelalgia

scientific article published on March 2014

Improving mutation screening in familial hematuric nephropathies through next generation sequencing

scientific article

Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?

scientific article published on 30 November 2011

KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes

scientific article

Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears

scientific article

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