C. Billon

Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome

C. Philippe, A. Piton, Y. Duffourd, 2023, American journal of medical genetics. Part A.

Assessment of arterial damage in vascular Ehlers-Danlos syndrome: A retrospective multicentric cohort

P. Boutouyrie, X. Jeunemaître, R. Bruno, 2022, Frontiers in Cardiovascular Medicine.