LR
Laure Raymond

Publications (2)

A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report
Article scientifique · 2018
Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease
Article scientifique · 2017

Domaines principaux

Sciences de la vie et biotechnologies1 Sciences de la santé1

Statistiques

Consultations6
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