VD
Valérie Delague

Publications (2)

Identification of a ERCC5 c.2333T>C (L778P) Variant in Two Tunisian Siblings With Mild Xeroderma Pigmentosum Phenotype
Article scientifique · 2019
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide withRAF1S259Y neomutation
Article scientifique · 2019

Domaines principaux

Sciences de la vie et biotechnologies2

Statistiques

Consultations2
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