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Results: 1-5 |
Results: 5

Authors: Houdayer, C Portnoi, MF Vialard, F Soupre, V Crumiere, C Taillemite, JL Couderc, R Vazquez, JP Bahuau, M
Citation: C. Houdayer et al., Pierre Robin sequence and interstitial deletion 2q32.3-q33.2, AM J MED G, 102(3), 2001, pp. 219-226

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: Abdelmoula, NB Portnoi, MF Vialard, F Amouri, A Van den Akker, J Taillemite, JL
Citation: Nb. Abdelmoula et al., Molecular cytogenetic techniques: principles and advances, M S-MED SCI, 16(12), 2000, pp. 1405-1411

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
Risultati: 1-5 |