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Results: 1-6 |
Results: 6

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: Geoffroy-Perez, B Janin, N Ossian, K Lauge, A Croquette, MF Griscelli, C Debre, M Bressac-De-Paillerets, B Aurias, A Stoppa-Lyonnet, D Andrieu, N
Citation: B. Geoffroy-perez et al., Cancer risk in heterozygotes for ataxia-telangiectasia, INT J CANC, 93(2), 2001, pp. 288-293

Authors: Saccone, S Federico, C Solovei, I Croquette, MF Della Valle, G Bernardi, G
Citation: S. Saccone et al., Identification of the gene-richest bands in human prometaphase chromosomes, CHROMOS RES, 7(5), 1999, pp. 379-386

Authors: Breviere, GM Croquette, MF Delobel, B Pellerin, P Rey, C
Citation: Gm. Breviere et al., Conotruncal defects and other clinical aspects secondary to genotype 22q11deletion - Series of 111 cases, ARCH PED, 6, 1999, pp. 305S-307S

Authors: Manouvrier-Hanu, S Amiel, J Jacquot, S Merienne, K Moerman, A Coeslier, A Labarriere, F Vallee, L Croquette, MF Hanauer, A
Citation: S. Manouvrier-hanu et al., Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome, J MED GENET, 36(10), 1999, pp. 775-778

Authors: Janin, N Andrieu, N Ossian, K Lauge, A Croquette, MF Griscelli, C Debre, M Bressac-de-Paillerets, B Aurias, A Stoppa-Lyonnet, D
Citation: N. Janin et al., Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families, BR J CANC, 80(7), 1999, pp. 1042-1045
Risultati: 1-6 |