H. Pécheur

Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: a cytogenetic pitfall.

V. Biancalana, O. Caron, G. Rudolf, 2008, European journal of medical genetics.

VASCULAR IgA AND C3 DEPOSITION IN GASTROINTESTINAL TRACT OF PATIENTS WITH HENOCH-SCHONLEIN PURPURA

P. Babin, C. Matuchansky, G. Touchard, 1983, The Lancet.

De novo trisomy 22 due to an extra 22Q-chromosome.

C. Stoll, A. Schnebelen, H. Pécheur, 1997, Annales de genetique.