T. Gaillon

Fetal RhD genotyping by maternal serum analysis: a two-year experience.

A. Benachi, P. Ernault, Jean‐Marc Costa, 2005, American journal of obstetrics and gynecology.

Novel comprehensive diagnostic strategy in Pitt–Hopkins syndrome: Clinical score and further delineation of the TCF4 mutational spectrum

A. Afenjar, N. Philip, S. Aftimos, 2012, Human mutation.

TCF4 Deletions in Pitt‐Hopkins Syndrome

N. Philip, J. Rankin, F. Giuliano, 2008, Human mutation.

Chimeric LNA/DNA probes as a detection system for real-time PCR.

K. Arar, P. Ernault, Jean‐Marc Costa, 2004, Clinical biochemistry.

Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders

F. Giuliano, S. Amselem, A. Briand-Suleau, 2021, Molecular Psychiatry.