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Results:
1-10
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Results: 10
Authors:
Colleaux, L
Rio, M
Heuertz, S
Moindrault, S
Turleau, C
Ozilou, C
Gosset, P
Raoult, O
Lyonnet, S
Cormier-Daire, V
Amiel, J
Le Merrer, M
Picq, M
de Blois, MC
Prieur, M
Romana, S
Cornelis, F
Vekemans, M
Munnich, A
Citation: L. Colleaux et al., A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation, EUR J HUM G, 9(5), 2001, pp. 319-327
Authors:
Rio, M
Ozilou, C
Cormier-Daire, V
Turleau, C
Prieur, M
Vekemans, M
Chauveau, P
Munnich, A
Colleaux, L
Citation: M. Rio et al., Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation, HUM GENET, 108(6), 2001, pp. 511-515
Authors:
Joly, G
Lapierre, JM
Ozilou, C
Gosset, P
Aurias, A
de Blois, MC
Prieur, M
Raoul, O
Colleaux, L
Munnich, A
Romana, SP
Vekemans, M
Turleau, C
Citation: G. Joly et al., Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype, CLIN GENET, 60(3), 2001, pp. 212-219
Authors:
Cardoso, C
Mignon, C
Hetet, G
Grandchamps, B
Fontes, M
Colleaux, L
Citation: C. Cardoso et al., The human EZH2 gene: genomic organisation and revised mapping in 7q35 within the critical region for malignant myeloid disorders, EUR J HUM G, 8(3), 2000, pp. 174-180
Authors:
Langnaese, K
Colleaux, L
Kloos, DU
Fontes, M
Wieacker, P
Citation: K. Langnaese et al., Cloning of Z39Ig, a novel gene with immunoglobulin-like domains located onhuman chromosome X, BBA-GENE ST, 1492(2-3), 2000, pp. 522-525
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:
Cardoso, C
Lutz, Y
Mignon, C
Compe, E
Depetris, D
Mattei, MG
Fontes, M
Colleaux, L
Citation: C. Cardoso et al., ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein, J MED GENET, 37(10), 2000, pp. 746-751
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:
Ronce, N
Raynaud, M
Toutain, A
Moizard, MP
Colleaux, L
Gendrot, C
Briault, S
Moraine, C
Citation: N. Ronce et al., Evidence for a new X-linked mental retardation gene in Xp21-Xp22: Clinicaland molecular data in one family, AM J MED G, 83(2), 1999, pp. 132-137
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
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