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Results:
1-20
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Results: 20
Authors:
Gili, R
Bonneau, D
Citation: R. Gili et D. Bonneau, CCD measurements of visual double stars made with the 74 cm and 50 cm refractors of the Nice Observatory (2nd series), ASTRON ASTR, 378(3), 2001, pp. 954-957
Authors:
Le Contel, D
Valtier, JC
Bonneau, D
Citation: D. Le Contel et al., SIDONIE: A gateway for visual double stars studies, ASTRON ASTR, 377(2), 2001, pp. 496-498
Authors:
Mourard, D
Thureau, N
Abe, L
Berio, P
Blazit, A
Bonneau, D
Petrov, R
Vakili, F
Citation: D. Mourard et al., The G12T/REGAIN interferometer, CR AC S IV, 2(1), 2001, pp. 35-44
Authors:
Crisponi, L
Deiana, M
Loi, A
Chiappe, F
Uda, M
Amati, P
Bisceglia, L
Zelante, L
Nagaraja, R
Porcu, S
Ristaldi, MS
Marzella, R
Rocchi, M
Nicolino, M
Lienhardt-Roussie, A
Nivelon, A
Verloes, A
Schlessinger, D
Gasparini, P
Bonneau, D
Cao, A
Pilia, G
Citation: L. Crisponi et al., The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome, NAT GENET, 27(2), 2001, pp. 159-166
Authors:
Nishimura, DY
Searby, CC
Carmi, R
Elbedour, K
Van Maldergem, L
Fulton, AB
Lam, BL
Powell, BR
Swiderski, RE
Bugge, KE
Haider, NB
Kwitek-Black, AE
Ying, LH
Duhl, DM
Gorman, SW
Heon, E
Iannaccone, A
Bonneau, D
Biesecker, LG
Jacobson, SG
Stone, EM
Sheffield, VC
Citation: Dy. Nishimura et al., Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2), HUM MOL GEN, 10(8), 2001, pp. 865-874
Authors:
Giraudeau, F
Taine, L
Biancalana, V
Delobel, B
Journel, H
Missirian, C
Lacombe, D
Bonneau, D
Parent, P
Aubert, D
Hauck, Y
Croquette, MF
Toutain, A
Mattei, MG
Loiseau, HA
David, A
Vergnaud, G
Citation: F. Giraudeau et al., Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation, J MED GENET, 38(2), 2001, pp. 121-125
Authors:
Bonneau, D
Longy, M
Citation: D. Bonneau et M. Longy, Mutations of the human PTEN gene, HUM MUTAT, 16(2), 2000, pp. 109-122
Authors:
Optasanu, V
Bonneau, D
Citation: V. Optasanu et D. Bonneau, Finite element mass-conserving cavitation algorithm in pure squeeze motion. Validation/application to a connecting-rod small end bearing, J TRIBOL, 122(1), 2000, pp. 162-169
Authors:
Piffeteau, S
Souchet, D
Bonneau, D
Citation: S. Piffeteau et al., Influence of thermal and elastic deformations on connecting-rod big end bearing lubrication under dynamic loading, J TRIBOL, 122(1), 2000, pp. 181-191
Authors:
Sarfati, R
Hubert, A
Dugue-Marechaud, M
Biran-Mucignat, V
Pierre, F
Bonneau, D
Citation: R. Sarfati et al., Prenatal diagnosis of Gaucher's disease type 2. Ultrasonographic, biochemical and histological aspects, PRENAT DIAG, 20(4), 2000, pp. 340-343
Authors:
Merlini, L
Kaplan, JC
Navarro, C
Barois, A
Bonneau, D
Brasa, J
Echenne, B
Gallano, P
Jarre, L
Jeanpierre, M
Kalaydjieva, L
Leturcq, F
Levi-Gomes, A
Toutain, A
Tournev, I
Urtizberea, A
Vallat, JM
Voit, T
Warter, JM
Citation: L. Merlini et al., Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation, NEUROLOGY, 54(5), 2000, pp. 1075-1079
Authors:
Berio, P
Mourard, D
Bonneau, D
Chesneau, O
Stee, P
Thureau, N
Vakili, F
Borgnino, J
Citation: P. Berio et al., Spectrally resolved Michelson stellar interferometry. I. Exact formalism in the multispeckle mode, J OPT SOC A, 16(4), 1999, pp. 872-881
Authors:
Garnier, T
Bonneau, D
Grente, C
Citation: T. Garnier et al., Three-dimensional EHD behavior of the engine block/crankshaft assembly fora four cylinder inline automotive engine, J TRIBOL, 121(4), 1999, pp. 721-730
Authors:
Goizet, C
Bonneau, D
Lacombe, D
Citation: C. Goizet et al., W syndrome: Report of three cases and review, AM J MED G, 87(5), 1999, pp. 446-449
Authors:
Bonneau, D
Roume, J
Gonzalez, M
Toutain, A
Carles, D
Marechaud, M
Biran-Mucignat, V
Amati, P
Moraine, C
Citation: D. Bonneau et al., Splenogonadal fusion limb defect syndrome: Report of five new cases and review, AM J MED G, 86(4), 1999, pp. 347-358
Authors:
Bonneau, D
Marechaud, M
Odent, S
Piegay, I
Godard, A
Amati, P
Citation: D. Bonneau et al., Heterotaxy-neural tube defect and holoprosencephaly occurring independently in two sib fetuses, AM J MED G, 84(4), 1999, pp. 373-376
Authors:
Kraimps, JL
Canzian, F
Jost, C
Menet, E
Amati, P
Levillian, P
Harach, R
Lesueur, F
Barbier, J
Romeo, G
Bonneau, D
Citation: Jl. Kraimps et al., Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene, SURGERY, 126(6), 1999, pp. 1188-1194
Authors:
Harach, HR
Lesueur, F
Amati, P
Brown, A
Canzian, F
Kraimps, JL
Levillain, P
Menet, E
Romeo, G
Bonneau, D
Citation: Hr. Harach et al., Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2, J PATHOLOGY, 189(3), 1999, pp. 387-393
Authors:
Berio, P
Stee, P
Vakili, F
Mourard, D
Bonneau, D
Chesneau, O
Thureau, N
Le Mignant, D
Hirata, R
Citation: P. Berio et al., Interferometric insight into gamma Cassiopeiae long-term variability, ASTRON ASTR, 345(1), 1999, pp. 203-210
Authors:
Canzian, F
Amati, P
Harach, HR
Kraimps, JL
Lesueur, F
Barbier, J
Levillain, P
Romeo, G
Bonneau, D
Citation: F. Canzian et al., A gene predisposing to familial thyroid tumors with cell oxyphilia maps tochromosome 19p13.2, AM J HU GEN, 63(6), 1998, pp. 1743-1748
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