S. Chantot-Bastaraud

Further delineation of the MECP2 duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features

S. Julia, R. Touraine, A. Afenjar, 2018, Journal of Medical Genetics.

Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency.

B. Donadille, P. Touraine, C. Dodé, 2016, The Journal of clinical endocrinology and metabolism.

French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature.

B. Delobel, I. Luquet, F. Fellmann, 2002, Annales de genetique.