Authors:
Orti, R
Rachidi, M
Vialard, F
Toyama, K
Lopes, C
Taudien, S
Rosenthal, A
Yaspo, ML
Sinet, PM
Delabar, JM
Citation: R. Orti et al., Characterization of a novel gene, C21orf6, mapping to a critical region ofchromosome 21q22.1 involved in the monosomy 21 phenotype and of its murineortholog, orf5, GENOMICS, 64(2), 2000, pp. 203-210
Authors:
Vialard, F
Toyama, K
Vernoux, S
Carlson, EJ
Epstein, CJ
Sinet, PM
Rahmani, Z
Citation: F. Vialard et al., Overexpression of mSim2 gene in the zona limitans of the diencephalon of segmental trisomy 16 Ts1Cje fetuses, a mouse model for trisomy 21: a novel whole-mount based RNA hybridization study, DEV BRAIN R, 121(1), 2000, pp. 73-78
Authors:
Portnoi, MF
Bouayed-Abdelmoula, N
Mirc, M
Zemni, R
Castaing, H
Stephann, J
Ardalan, A
Vialard, F
Nouchy, M
Daoud, P
Chelly, J
Taillemite, JL
Citation: Mf. Portnoi et al., Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation, CLIN GENET, 58(2), 2000, pp. 116-122