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Results:
1-8
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Results: 8
Authors:
Couvert, P
Bienvenu, T
Aquaviva, C
Poirier, K
Moraine, C
Gendrot, C
Verloes, A
Andres, C
Le Fevre, AC
Souville, I
Steffann, J
des Portes, V
Ropers, HH
Yntema, HG
Fryns, JP
Briault, S
Chelly, J
Cherif, B
Citation: P. Couvert et al., MECP2 is highly mutated in X-linked mental retardation, HUM MOL GEN, 10(9), 2001, pp. 941-946
Authors:
Raynaud, M
Moizard, MP
Dessay, B
Briault, S
Toutain, A
Gendrot, C
Ronce, N
Moraine, C
Citation: M. Raynaud et al., Systematic analysis of X-inactivation in 19XLMR families: extremely skewedprofiles in carriers in three families, EUR J HUM G, 8(4), 2000, pp. 253-258
Authors:
Briault, S
Villard, L
Rogner, U
Coy, J
Odent, S
Lucas, J
Passage, E
Zhu, DP
Shrimpton, A
Pembrey, M
Till, M
Guichet, A
Dessay, S
Fontes, M
Poustka, A
Moraine, C
Citation: S. Briault et al., Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]?, AM J MED G, 95(2), 2000, pp. 178-181
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:
Forissier, JF
Richard, P
Briault, S
Ledeuil, C
Dubourg, O
Charbonnier, B
Carrier, L
Moraine, C
Bonne, G
Komajda, M
Schwartz, K
Hainque, B
Citation: Jf. Forissier et al., First description of germline mosaicism in familial hypertrophic cardiomyopathy, J MED GENET, 37(2), 2000, pp. 132-134
Authors:
Briault, S
Odent, S
Lucas, J
Le Merrer, M
Turleau, C
Munnich, A
Moraine, C
Citation: S. Briault et al., Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome, AM J MED G, 86(2), 1999, pp. 112-114
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
Risultati:
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