Monosomy 18p

Por Turleau, Catherine
Publicado em 2008

Distal Xq duplication and functional Xq disomy

Por Sanlaville, Damien, Schluth-Bolard, Caroline, Turleau, Catherine
Publicado em 2009

A new G to T polymorphism in the retinoblastoma gene RB1 detected by DGGE

Por Blanquet, Véronique, Turleau, Catherine, Goossens, Michel, Besmond, Claude
Publicado em 1992

Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition

Por Rio, Marlène, Malan, Valérie, Boissel, Sarah, Toutain, Annick, Royer, Ghislaine, Gobin, Stéphanie, Morichon-Delvallez, Nicole, Turleau, Catherine, Bonnefont, Jean-Paul, Munnich, Arnold, Vekemans, Michel, Colleaux, Laurence
Publicado em 2010

Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome

Por Lüdecke, Hermann-Josef, Johnson, Carey, Wagner, Michael J., Wells, Dan E., Turleau, Catherine, Tommerup, Niels, Latos-Bielenska, Anna, Sandig, Klaus-Rainer, Meinecke, Peter, Zabel, Bernhard, Horsthemke, Bernhard
Publicado em 1991

Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth

Por Malan, Valérie, Chevallier, Suzanne, Soler, Gwendoline, Coubes, Christine, Lacombe, Didier, Pasquier, Laurent, Soulier, Jean, Morichon-Delvallez, Nicole, Turleau, Catherine, Munnich, Arnold, Romana, Serge, Vekemans, Michel, Cormier-Daire, Valérie, Colleaux, Laurence
Publicado em 2010