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Citation: C. Marcelis et al., Wolf-Hirschhorn (4p) syndrome in adults, GEN COUNSEL, 12(1), 2001, pp. 35-48

Authors: Giraudeau, F Taine, L Biancalana, V Delobel, B Journel, H Missirian, C Lacombe, D Bonneau, D Parent, P Aubert, D Hauck, Y Croquette, MF Toutain, A Mattei, MG Loiseau, HA David, A Vergnaud, G

Citation: F. Giraudeau et al., Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation, J MED GENET, 38(2), 2001, pp. 121-125

Authors: Missirian, C Moncla, A Voelckel, MA Ravix, V Philip, N

Citation: C. Missirian et al., Fragile X syndrome and 22q11.2 microdeletion in the same sibship, AM J MED G, 95(4), 2000, pp. 358-360

Authors: Chauve, X Missirian, C Malzac, P Girardot, L Guys, JM Louis, C Philip, N Voelckel, MA

Citation: X. Chauve et al., Genetic homogeneity of the urofacial (Ochoa) syndrome confirmed in a new French family, AM J MED G, 95(1), 2000, pp. 10-12