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:
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