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Results:
1-14
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Results: 14
Authors:
Vourc'h, P
Bienvenu, T
Beldjord, C
Chelly, J
Barthelemy, C
Muh, JP
Andres, C
Citation: P. Vourc'H et al., No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients, EUR J HUM G, 9(7), 2001, pp. 556-558
Authors:
Girard, M
Couvert, P
Carrie, A
Tardieu, M
Chelly, J
Beldjord, C
Bienvenu, T
Citation: M. Girard et al., Parental origin of de novo MECP2 mutations in Rett syndrome, EUR J HUM G, 9(3), 2001, pp. 231-236
Authors:
Bienvenu, T
Carrie, A
de Roux, N
Vinet, MC
Jonveaux, P
Couvert, P
Villard, L
Arzimanoglou, A
Beldjord, C
Fontes, M
Tardieu, M
Chelly, J
Citation: T. Bienvenu et al., MECP2 mutations account for most cases of typical forms of Rett syndrome, HUM MOL GEN, 9(9), 2000, pp. 1377-1384
Authors:
Bienvenu, T
des Portes, V
McDonell, N
Carrie, A
Zemni, R
Couvert, P
Ropers, HH
Moraine, C
van Bokhoven, H
Fryns, JP
Allen, K
Walsh, CA
Boue, J
Kahn, A
Chelly, J
Beldjord, C
Citation: T. Bienvenu et al., Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation, AM J MED G, 93(4), 2000, pp. 294-298
Authors:
Lucas, H
Patrat, C
Jouannet, P
Beldjord, C
Bienvenu, T
Citation: H. Lucas et al., A novel, rapid, and accurate method for detecting microdeletion involving the DAZ gene in infertile men, FERT STERIL, 73(2), 2000, pp. 242-247
Authors:
Billuart, P
Chelly, J
Carrie, A
Vinet, MC
Couvert, P
McDonell, N
Zemni, R
Kahn, A
Moraine, C
Beldjord, C
Bienvenu, T
Citation: P. Billuart et al., Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation, ANN GENET, 43(1), 2000, pp. 5-9
Authors:
Carrie, A
Jun, L
Bienvenu, T
Vinet, MC
McDonell, N
Couvert, P
Zemni, R
Cardona, A
Van Buggenhout, G
Frints, S
Hamel, B
Moraine, C
Ropers, HH
Strom, T
Howell, GR
Whittaker, A
Ross, MT
Kahn, A
Fryns, JP
Beldjord, C
Marynen, P
Chelly, J
Citation: A. Carrie et al., A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation, NAT GENET, 23(1), 1999, pp. 25-31
Authors:
Carrie, A
Nepotes, V
Billuart, P
Beldjord, C
Bienvenu, T
Chelly, J
Bruls, T
Heilig, R
Weissenbach, J
Jun, L
Marynen, P
Citation: A. Carrie et al., Construction of a highly annotated cosmid contig spanning 550 kb within the X-linked non-specific mental retardation candidate region at Xp21.3-22.1, AM J MED G, 85(3), 1999, pp. 252-254
Authors:
des Portes, V
Beldjord, C
Chelly, J
Hamel, B
Kremer, H
Smits, A
van Bokhoven, H
Ropers, HH
Claes, S
Fryns, JP
Ronce, N
Gendrot, C
Toutain, A
Raynaud, M
Moraine, C
Citation: V. Des Portes et al., X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: The European XLMR Consortium, AM J MED G, 85(3), 1999, pp. 263-265
Authors:
Ben Jemaa, L
des Portes, V
Zemni, R
Mrad, R
Maazoul, F
Beldjord, C
Chaabouni, H
Chelly, J
Citation: L. Ben Jemaa et al., Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54), AM J MED G, 85(3), 1999, pp. 276-282
Authors:
Rodriguez-Macias, KA
Thibaud, E
Houang, M
Duflos, C
Beldjord, C
Rappaport, R
Citation: Ka. Rodriguez-macias et al., Follow up of precocious pseudopuberty associated with isolated ovarian follicular cysts, ARCH DIS CH, 81(1), 1999, pp. 53-56
Authors:
Elbaz, A
Suedois, J
Duquesnoy, M
Beldjord, C
Berchel, C
Merault, G
Citation: A. Elbaz et al., Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies, J INTEL DIS, 42, 1998, pp. 81-89
Authors:
Billuart, P
Bienvenu, T
Ronce, N
Des Portes, V
Vinet, MC
Zemni, R
Carrie, A
Beldjord, C
Kahn, A
Moraine, C
Chelly, J
Citation: P. Billuart et al., Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation., PATH BIOL, 46(9), 1998, pp. 678-678
Authors:
Steffann, J
Vidaud, D
Bousquet, S
Jullien, M
Ninot, A
Kaplan, JC
Beldjord, C
Bienvenu, T
Citation: J. Steffann et al., Novel double mutant CF allele identified in a cystic fibrosis patient withmeconium ileus., ANN GENET, 41(4), 1998, pp. 213-215
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