Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21 von Hibaoui, Youssef, Grad, Iwona, Letourneau, Audrey, Sailani, M Reza, Dahoun, Sophie, Santoni, Federico A, Gimelli, Stefania, Guipponi, Michel, Pelte, Marie Françoise, Béna, Frédérique, Antonarakis, Stylianos E, Feki, Anis

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Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome von Schneider, Maude, Van der Linden, Martial, Glaser, Bronwyn, Rizzi, Eleonora, Dahoun, Sophie P, Hinard, Christine, Bartoloni, Lucia, Antonarakis, Stylianos E, Debbané, Martin, Eliez, Stephan

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No Evidence for an Effect of COMT Val158Met Genotype on Executive Function in Patients With 22q11 Deletion Syndrome von Glaser, Bronwyn, Debbane, Martin, Hinard, Christine, Morris, Michael A., Dahoun, Sophie P., Antonarakis, Stylianos E., Eliez, Stephan

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Parental decisions following the prenatal diagnosis of sex chromosome abnormalities von Hamamy, Hanan A, Dahoun, Sophie

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Language skills in children with velocardiofacial syndrome (deletion 22q11.2) von Glaser, Bronwyn, Mumme, Donna L., Blasey, Christine, Morris, Michael A., Dahoun, Sophie P., Antonarakis, Stylianos E., Reiss, Allan L., Eliez, Stephan

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Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus von Birraux, Jacques, Mouafo, Faustin Tambo, Dahoun, Sophie, Tardy, Veronique, Morel, Yves, Mouriquand, Pierre, Le Coultre, Claude, Mure, Pierre-Yves

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Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report von Hamamy, Hanan, Antonarakis, Stylianos E, Cavalli-Sforza, Luigi Luca, Temtamy, Samia, Romeo, Giovanni, Kate, Leo P Ten, Bennett, Robin L, Shaw, Alison, Megarbane, Andre, van Duijn, Cornelia, Bathija, Heli, Fokstuen, Siv, Engel, Eric, Zlotogora, Joel, Dermitzakis, Emmanouil, Bottani, Armand, Dahoun, Sophie, Morris, Michael A, Arsenault, Steve, Aglan, Mona S, Ajaz, Mubasshir, Alkalamchi, Ayad, Alnaqeb, Dhekra, Alwasiyah, Mohamed K, Anwer, Nawfal, Awwad, Rawan, Bonnefin, Melissa, Corry, Peter, Gwanmesia, Lorraine, Karbani, Gulshan A, Mostafavi, Maryam, Pippucci, Tommaso, Ranza-Boscardin, Emmanuelle, Reversade, Bruno, Sharif, Saghira M, Teeuw, Marieke E, Bittles, Alan H

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Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21 von LYLE, Robert, BENA, Frédérique, DOCO-FENZY, Martine, CORNILLET-LEFEBVRE, Pascale, PELET, Anna, LYONNET, Stanislas, TOUTAIN, Annick, COLLEAUX, Laurence, HORST, Jürgen, KENNERKNECHT, Ingo, WAKAMATSU, Nobuaki, DESCARTES, Maria, GAGOS, Sarantis, FRANKLIN, Judy C, FLORENTIN-ARAR, Lina, KITSIOU, Sophia, AIT YAHYA-GRAISON, Emilie, COSTANTINE, Maher, SINET, Pierre-Marie, DELABAR, Jean M, ANTONARAKIS, Stylianos E, GEHRIG, Corinne, LOPEZ, Gipsy, SCHINZEL, Albert, LESPINASSE, James, BOTTANI, Armand, DAHOUN, Sophie, TAINE, Laurence

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Establishment of permanent cell lines purified from human mesothelioma: morphological aspects, new marker expression and karyotypic analysis von Philippeaux, Marie-Marthe, Pache, Jean-Claude, Dahoun, Sophie, Barnet, Marc, Robert, John-Henri, Mauël, Jacques, Spiliopoulos, Anastase

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Unusually stable abnormal karyotype in a highly aggressive melanoma negative for telomerase activity von Gagos, Sarantis, Papaioannou, George, Chiourea, Maria, Merk-Loretti, Sophie, Jefford, Charles-Edward, Mikou, Panagiota, Irminger-Finger, Irmgard, Liossi, Anna, Blouin, Jean-Louis, Dahoun, Sophie

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MECP2 duplication syndrome in a patient from Cameroon von Tekendo‐Ngongang, Cedrik, Dahoun, Sophie, Nguefack, Séraphin, Moix, Isabelle, Gimelli, Stefania, Zambo, Huguette, Morris, Michael A., Sloan‐Béna, Frédérique, Wonkam, Ambroise

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Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes von Delio, Maria, Guo, Tingwei, McDonald-McGinn, Donna M., Zackai, Elaine, Herman, Sean, Kaminetzky, Mark, Higgins, Anne Marie, Coleman, Karlene, Chow, Carolyn, Jarlbrzkowski, Maria, Bearden, Carrie E., Bailey, Alice, Vangkilde, Anders, Olsen, Line, Olesen, Charlotte, Skovby, Flemming, Werge, Thomas M., Templin, Ludivine, Busa, Tiffany, Philip, Nicole, Swillen, Ann, Vermeesch, Joris R., Devriendt, Koen, Schneider, Maude, Dahoun, Sophie, Eliez, Stephan, Schoch, Kelly, Hooper, Stephen R., Shashi, Vandana, Samanich, Joy, Marion, Robert, van Amelsvoort, Therese, Boot, Erik, Klaassen, Petra, Duijff, Sasja N., Vorstman, Jacob, Yuen, Tracy, Silversides, Candice, Chow, Eva, Bassett, Anne, Frisch, Amos, Weizman, Abraham, Gothelf, Doron, Niarchou, Maria, van den Bree, Marianne, Owen, Michael J., Suñer, Damian Heine, Andreo, Jordi Rosell, Armando, Marco, Vicari, Stefano, Digilio, Maria Cristina, Auton, Adam, Kates, Wendy R., Wang, Tao, Shprintzen, Robert J., Emanuel, Beverly S., Morrow, Bernice E.

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The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon von Wonkam, Ambroise, Toko, Ricardo, Chelo, David, Tekendo-Ngongang, Cedrik, Kingue, Samuel, Dahoun, Sophie

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The 22q11.2 Deletion Syndrome in Congenital Heart Defects von Wonkam, Ambroise, Toko, Ricardo, Chelo, David, Tekendo-Ngongang, Cedrik, Kingue, Samuel, Dahoun, Sophie

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Challenges in Clinical Diagnosis of Williams-Beuren Syndrome in Sub-Saharan Africans: Case Reports from Cameroon von Tekendo-Ngongang, Cedrik, Dahoun, Sophie, Nguefack, Seraphin, Gimelli, Stefania, Sloan-Béna, Frédérique, Wonkam, Ambroise

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Initiation of a medical genetics service in sub-Saharan Africa: Experience of prenatal diagnosis in Cameroon von Wonkam, Ambroise, Tekendo, Cedrik Ngongang, Sama, Dohbit Julius, Zambo, Huguette, Dahoun, Sophie, Béna, Frédérique, Morris, Michael A

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Mechanisms Regulating the Proliferative Potential of Human CD8+ T Lymphocytes Overexpressing Telomerase von Menzel, Olivier, Migliaccio, Marco, Goldstein, Darlene R, Dahoun, Sophie, Delorenzi, Mauro, Rufer, Nathalie

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Initiation of prenatal genetic diagnosis of chromosomal anomalies in Cameroon von Wonkam, Ambroise, Zambo, Huguette, Tekendo, Cedrik Ngongang, Béna, Frédérique, Dahoun, Sophie

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Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome von Schneider, Maude, Van der Linden, Martial, Glaser, Bronwyn, Rizzi, Eleonora, Dahoun, Sophie P, Hinard, Christine, Bartoloni, Lucia, Antonarakis, Stylianos E, Debbané, Martin, Eliez, Stephan

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Derivation of the first Swiss human embryonic stem cell line from a single blastomere of an arrested four-cell stage embryo von Feki, Anis, Bosman, Alexis, Dubuisson, Jean-Bernard, Irion, Olivier, Dahoun, Sophie, Pelte, Marie-Françoise, Hovatta, Outi, Jaconi, Marisa E

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