检索结果 - Arbogast, Thomas

Deletion of the App-Runx1 region in mice models human partial monosomy 21 由 Arbogast, Thomas, Raveau, Matthieu, Chevalier, Claire, Nalesso, Valérie, Dembele, Doulaye, Jacobs, Hugues, Wendling, Olivia, Roux, Michel, Duchon, Arnaud, Herault, Yann

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Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies 由 Harel, Tamar, Griffin, John N, Arbogast, Thomas, Monroe, Tanner O, Palombo, Flavia, Martinelli, Marcella, Seri, Marco, Pippucci, Tommaso, Elpeleg, Orly, Katsanis, Nicholas

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The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs 由 Loviglio, Maria Nicla, Arbogast, Thomas, Jønch, Aia Elise, Collins, Stephan C., Popadin, Konstantin, Bonnet, Camille S., Giannuzzi, Giuliana, Maillard, Anne M., Jacquemont, Sébastien, Yalcin, Binnaz, Katsanis, Nicholas, Golzio, Christelle, Reymond, Alexandre

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Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions 由 Arbogast, Thomas, Razaz, Parisa, Ellegood, Jacob, McKinstry, Spencer U, Erdin, Serkan, Currall, Benjamin, Aneichyk, Tanya, Lerch, Jason P, Qiu, Lily R, Rodriguiz, Ramona M, Henkelman, R M, Talkowski, Michael E, Wetsel, William C, Golzio, Christelle, Katsanis, Nicholas

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Germline-Activating RRAS2 Mutations Cause Noonan Syndrome 由 Niihori, Tetsuya, Nagai, Koki, Fujita, Atsushi, Ohashi, Hirofumi, Okamoto, Nobuhiko, Okada, Satoshi, Harada, Atsuko, Kihara, Hirotaka, Arbogast, Thomas, Funayama, Ryo, Shirota, Matsuyuki, Nakayama, Keiko, Abe, Taiki, Inoue, Shin-ichi, Tsai, I-Chun, Matsumoto, Naomichi, Davis, Erica E., Katsanis, Nicholas, Aoki, Yoko

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Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development 由 Qiu, Yuqi, Arbogast, Thomas, Lorenzo, Sandra Martin, Li, Hongying, Tang, Shih C., Richardson, Ellen, Hong, Oanh, Cho, Shawn, Shanta, Omar, Pang, Timothy, Corsello, Christina, Deutsch, Curtis K., Chevalier, Claire, Davis, Erica E., lakoucheva, Lilia M., Herault, Yann, Katsanis, Nicholas, Messer, Karen, Sebat, Jonathan

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Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition 由 Arbogast, Thomas, Iacono, Giovanni, Chevalier, Claire, Afinowi, Nurudeen O., Houbaert, Xander, van Eede, Matthijs C., Laliberte, Christine, Birling, Marie-Christine, Linda, Katrin, Meziane, Hamid, Selloum, Mohammed, Sorg, Tania, Nadif Kasri, Nael, Koolen, David A., Stunnenberg, Henk G., Henkelman, R. Mark, Kopanitsa, Maksym, Humeau, Yann, De Vries, Bert B. A., Herault, Yann

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