Viviana Granados

Molecular genetic diagnosis of Tunisian Glanzmann thrombasthenia patients reveals a common nonsense mutation in the ITGA2B gene that seems to be specific for the studied population

C. Aloui, S. Laradi, O. Garraud, 2018, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Development of a highly resolutive method, using a double quadruplex tetra-primer-ARMS-PCR coupled with capillary electrophoresis to study CD40LG polymorphisms.

C. Aloui, S. Laradi, O. Garraud, 2015, Molecular and cellular probes.

Confirmation that RIPK4 mutations cause not only Bartsocas‐Papas syndrome but also CHAND syndrome

R. Touraine, N. Philip, M. Jeraiby, 2017, American journal of medical genetics. Part A.

Development of a highly resolutive method, using a double quadruplex tetra-primer-ARMS-PCR coupled with capillary electrophoresis to study CD40LG polymorphisms.

C. Aloui, S. Laradi, O. Garraud, 2015, Molecular and cellular probes.