Contiguous Gene Deletion within Chromosome Arm 10q Is Associated with Juvenile Polyposis of Infancy, Reflecting Cooperation between the BMPR1A and PTEN Tumor-Suppressor Genes von Delnatte, Capucine, Sanlaville, Damien, Mougenot, Jean-François, Vermeesch, Joris-Robert, Houdayer, Claude, Blois, Marie-Christine de, Genevieve, David, Goulet, Olivier, Fryns, Jean-Pierre, Jaubert, Francis, Vekemans, Michel, Lyonnet, Stanislas, Romana, Serge, Eng, Charis, Stoppa-Lyonnet, Dominique

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Clinical and molecular delineation of Tetrasomy 9p syndrome: Report of 12 new cases and literature review von El Khattabi, Laïla, Jaillard, Sylvie, Andrieux, Joris, Pasquier, Laurent, Perrin, Laurence, Capri, Yline, Benmansour, Abdelmadjid, Toutain, Annick, Marcorelles, Pascale, Vincent-Delorme, Catherine, Journel, Hubert, Henry, Catherine, De Barace, Claire, Devisme, Louise, Dubourg, Christèle, Demurger, Florence, Lucas, Josette, Belaud-Rotureau, Marc-Antoine, Amiel, Jeanne, Malan, Valérie, De Blois, Marie-Christine, De Pontual, Loïc, Lebbar, Aziza, Le DÛ, Nathalie, Germain, Dominique P., Pinard, Jean-Marc, Pipiras, Eva, Tabet, Anne-Claude, Aboura, Azzedine, Verloes, Alain

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Functional disomy of the Xq28 chromosome region von SANLAVILLE, Damien, PRIEUR, Marguerite, CORMIER-DAIRE, Valerie, BAUJAT, Genevieve, ROMANA, Serge, VEKEMANS, Michel, TURLEAU, Catherine, DE BLOIS, Marie-Christine, GENEVIEVE, David, LAPIERRE, Jean-Michel, OZILOU, Catherine, PICQ, Monique, GOSSET, Philippe, MORICHON-DELVALLEZ, Nicole, MUNNICH, Arnold

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Neurobehavioral Profile and Brain Imaging Study of the 22q13.3 Deletion Syndrome in Childhood von Philippe, Anne, Boddaert, Nathalie, Vaivre-Douret, Laurence, Robel, Laurence, Danon-Boileau, Laurent, Malan, Valerie, de Blois, Marie-Christine, Heron, Delphine, Colleaux, Laurence, Golse, Bernard, Zilbovicius, Monica, Munnich, Arnold

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Reply to Salviati et al von Sanlaville, Damien, Delnatte, Capucine, Mougenot, Jean-François, Vermeesch, Joris-Robert, Houdayer, Claude, de Blois, Marie-Christine, Genevieve, David, Goulet, Olivier, Fryns, Jean-Pierre, Jaubert, Francis, Vekemans, Michel, Lyonnet, Stanislas, Romana, Serge, Eng, Charis, Stoppa-Lyonnet, Dominique

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Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome von De Leersnyder, Hélène, de Blois, Marie-Christine, Claustrat, Bruno, Romana, Serge, Albrecht, Urs, von Kleist-Retzow, Jürgen-Christoph, Delobel, Bruno, Viot, Géraldine, Lyonnet, Stanislas, Vekemans, Michel, Munnich, Arnold

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Werner mesomelic dysplasia with Hirschsprung disease von Goldenberg, Alice, Milh, Mathieu, de Lagausie, Pascal, Mesnage, Renaud, Benarif, Fatiha, De Blois, Marie‐Christine, Munnich, Arnold, Lyonnet, Stanislas, Cormier‐Daire, Valérie

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Ebstein anomaly associated with rearrangements of chromosomal region 11q von de Lonlay-Debeney, Pascale, de Blois, Marie-Christine, Bonnet, Damien, Amiel, Jeanne, Abadie, Véronique, Picq, Monique, Lyonnet, Stanislas, Sidi, Daniel, Munnich, Arnold, Vekemans, Michel, Cormier-Daire, Valérie

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Failure to detect an 8p22-8p23.1 duplication in patients with Kabuki (Niikawa-Kuroki) syndrome von SANLAVILLE, Damien, GENEVIEVE, David, PARENT, Philippe, PRIEUR, Fabienne, PRIEUR, Marguerite, RAOUL, Odile, TOUTAIN, Annick, VERLOES, Alain, VIOT, Géraldine, ROMANA, Serge, MUNNICH, Arnold, LYONNET, Stanislas, BERNARDIN, Céline, VEKEMANS, Michel, TURLEAU, Catherine, AMIEL, Jeanne, BAUMANN, Clarisse, DE BLOIS, Marie-Christine, CORMIER-DAIRE, Valérie, GERARD, Bénédicte, GERARD, Marion, LE MERRER, Martine

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A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation von Colleaux, L, Rio, M, Heuertz, S, Moindrault, S, Turleau, C, Ozilou, C, Gosset, P, Raoult, O, Lyonnet, S, Cormier-Daire, V, Amiel, J, Le Merrer, M, Picq, M, de Blois, M C, Prieur, M, Romana, S, Cornelis, F, Vekemans, M, Munnich, A

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Characterization of a human ovarian adenocarcinoma line, IGROV1, in tissue culture and in nude mice von BENARD, J, DA SILVA, J, DE BLOIS, M.-C, BOYER, P, DUVILLARD, P, CHIRIC, E, RIOU, G

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A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH von Poirsier, Céline, Besseau-Ayasse, Justine, Schluth-Bolard, Caroline, Toutain, Jérôme, Missirian, Chantal, Le Caignec, Cédric, Bazin, Anne, de Blois, Marie Christine, Kuentz, Paul, Catty, Marie, Choiset, Agnès, Plessis, Ghislaine, Basinko, Audrey, Letard, Pascaline, Flori, Elisabeth, Jimenez, Mélanie, Valduga, Mylène, Landais, Emilie, Lallaoui, Hakima, Cartault, François, Lespinasse, James, Martin-Coignard, Dominique, Callier, Patrick, Pebrel-Richard, Céline, Portnoi, Marie-France, Busa, Tiffany, Receveur, Aline, Amblard, Florence, Yardin, Catherine, Harbuz, Radu, Prieur, Fabienne, Le Meur, Nathalie, Pipiras, Eva, Kleinfinger, Pascale, Vialard, François, Doco-Fenzy, Martine

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Identification of the IRXB gene cluster as candidate genes in severe dysgenesis of the ocular anterior segment von Chaabouni, Myriam, Etchevers, Heather, De Blois, Marie Christine, Calvas, Patrick, Waill-Perrier, Marie Christine, Vekemans, Michel, Romana, Serge Pierrick

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Absent lacrimal ducts, distichiasis, dysmorphic features, and brachydactyly: a case report von Holder-Espinasse, M, de Blois, M C, Faivre, L, Romana, S, Uteza, Y, Munnich, A, Lyonnet, S, Cormier-Daire, V, Amiel, J

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β1-adrenergic antagonists improve sleep and behavioural disturbances in a circadian disorder, Smith-Magenis syndrome von De Leersnyder, Hélène, de Blois, Marie-Christine, Vekemans, Michel, Sidi, Daniel, Villain, Elisabeth, Kindermans, Catherine, Munnich, Arnold

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Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization of 11 cases von Morleo, Manuela, Pramparo, Tiziano, Perone, Lucia, Gregato, Giuliana, Caignec, Cedric Le, Mueller, Robert F., Ogata, Tsutomu, Raas-Rothschild, Annick, de Blois, Marie Christine, Wilson, Louise C., Zaidman, Gerald, Zuffardi, Orsetta, Ballabio, Andrea, Franco, Brunella

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Homocysteine and the methotrexate toxicity in trisomy 21 von LEJEUNE, J, PEETERS, M, RETHORE, M.-O, DE BLOIS, M.-C

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adrenergic antagonists improve sleep and behavioural disturbances in a circadian disorder, Smith-Magenis syndrome von Leersnyder, Helene De, Blois, Marie-Christine de, Vekemans, Michel, Sidi, Daniel, Villain, Elisabeth, Kindermans, Catherine, Munnich, Arnold

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DNA polymorphism analysis in families with recurrence of free trisomy 21 von Pangalos, Constantinos G, Talbot Jr., Conover C, Lewis, John G, Adelsberger, Patricia A, Petersen, Michael B, Serre, Jean-Louis, Rethoré, Marie-Odile, de Blois, Marie-Christine, Parent, Philipe, Schinzel, Albert A, Binkert, Franz, Boue, Joelle, Corbin, Elisabeth, Croquette, M F, Gilgenkrantz, Simone, de Grouchy, Jean, Bertheas, M F, Prieur, Marguerite, Raoul, Odile, Serville, Framcoise, Siffroi, J P, Thepot, Francois, Lejeune, Jerome, Antonarakis, Stylianos E

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Werner mesomelic dysplasia with Hirschsprung disease von Goldenberg, Alice, Milh, Mathieu, de Lagausie, Pascal, Mesnage, Renaud, Benarif, Fatiha, De Blois, Marie-Christine, Munnich, Arnold, Lyonnet, Stanislas, Cormier-Daire, Valérie

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