Authors:
Lossi, AM
Colleaux, L
Chiaroni, P
Fontes, M
Villard, L
Abidi, F
Schwartz, C
Briault, S
Moraine, C
Citation: Am. Lossi et al., Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three families, AM J MED G, 94(5), 2000, pp. 386-388
Authors:
Villard, L
Belougne, J
Lossi, AM
Fontes, M
Colleaux, L
Citation: L. Villard et al., Transcript map of the human chromosome Xq11-Xq21 region: localization of 33 novel genes and one pseudogene, GENE, 235(1-2), 1999, pp. 43-50
Authors:
Villard, L
Bonino, MC
Abidi, F
Ragusa, A
Belougne, J
Lossi, AM
Seaver, L
Bonnefont, JP
Romano, C
Fichera, M
Lacombe, D
Hanauer, A
Philip, N
Schwartz, C
Fontes, M
Citation: L. Villard et al., Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome, J MED GENET, 36(3), 1999, pp. 183-186
Authors:
Villard, L
Briault, S
Lossi, AM
Paringaux, C
Belougne, J
Colleaux, L
Pincus, DR
Woollatt, E
Lespinasse, J
Munnich, A
Moraine, C
Fontes, H
Gecz, J
Citation: L. Villard et al., Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1, J MED GENET, 36(10), 1999, pp. 754-758
Authors:
Lossi, AM
Millan, JM
Villard, L
Orellana, C
Cardoso, C
Prieto, F
Fontes, M
Martinez, F
Citation: Am. Lossi et al., Mutation of the XNP/ATR-X gene in a family with severe mental retardation,spastic paraplegia and skewed pattern of X inactivation: Demonstration that the mutation is involved in the inactivation bias, AM J HU GEN, 65(2), 1999, pp. 558-562