Authors: Lucotte, G Semonin, O Mercier, G

Citation: G. Lucotte et al., Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1 in a French family, GEN COUNSEL, 12(2), 2001, pp. 173-175

Authors: Semonin, O Fontaine, K Daviaud, C Ayuso, C Lucotte, G

Citation: O. Semonin et al., Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva, AM J MED G, 102(4), 2001, pp. 314-317

Authors: Lucotte, G Bathelier, C Mercier, G Gerard, N Lenoir, G Semonin, O Fontaine, K

Citation: G. Lucotte et al., Localization of the gene for fibrodysplasia ossificans progressiva (FOP) to chromosome 17q21-22, GEN COUNSEL, 11(4), 2000, pp. 329-334

Authors: Lucotte, G Semonin, O Lutz, P

Citation: G. Lucotte et al., A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient, CLIN GENET, 56(6), 1999, pp. 469-470