Franck Bourdeaut

Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort

G. Leverger, F. Andreiuolo, L. Guerrini-Rousseau, 2015, Journal of Medical Genetics.

Malformations, genetic abnormalities, and wilms tumor

H. Brisse, D. Stoppa-Lyonnet, C. Baumann, 2014, Pediatric blood & cancer.

Glioma oncogenesis in the Constitutional mismatch repair deficiency (CMMRD) syndrome

S. Puget, F. Andreiuolo, L. Guerrini-Rousseau, 2024, Neuro-oncology advances.

Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.

S. Lyonnet, I. Janoueix-Lerosey, D. Trochet, 2007, European journal of cancer.