Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid von Essaoui, M, Nizon, M, Beaujard, M.P, Carrier, A, Tantau, J, de Blois, M.C, Fontaine, S, Michot, C, Amiel, J, Bernard, J.P, Attié-Bitach, T, Vekemans, M, Turleau, C, Ville, Y, Malan, V

Volltext

Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region von Chaabouni, M., Le Merrer, M., Raoul, O., Prieur, M., de Blois, M.C., Philippe, A., Vekemans, M., Romana, S.P.

Volltext

Deletion of the SIM1 gene von Faivre, L, Cormier-Daire, V, Lapierre, J.M, Colleaux, L, Jacquemont, S, Genevieve, D, Saunier, P, Munnich, A, Turleau, C, Romana, S, Prieur, M, Blois, M.C. De, Vekemans, M

Volltext

DNA POLYMORPHISM ANALYSIS IN FAMILIES WITH RECURRENCE OF FREE TRISOMY-21 von PANGALOS, CG, TALBOT, CC, LEWIS, JG, ADELSBERGER, PA, PETERSEN, MB, SERRE, JL, RETHORE, MO, DEBLOIS, MC, PARENT, P, SCHINZEL, AA, BINKERT, F, BOUE, J, CORBIN, E, CROQUETTE, MF, GILGENKRANTZ, S, DEGROUCHY, J, BERTHEAS, MF, PRIEUR, M, RAOUL, O, SERVILLE, F, SIFFROI, JP, THEPOT, F, LEJEUNE, J, ANTONARAKIS, SE

Volltext