Search Results - Depienne, Christel

Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity by Kalm, Tassja (Author) , Schob, Claudia (Author) , Völler, Hanna (Author) , Gardeitchik, Thatjana (Author) , Gilissen, Christian (Author) , Pfundt, Rolph (Author) , Klöckner, Chiara (Author) , Platzer, Konrad (Author) , Klabunde-Cherwon, Annick (Author) , Ries, Markus (Author) , Syrbe, Steffen (Author) , Beccaria, Francesca (Author) , Madia, Francesca (Author) , Scala, Marcello (Author) , Zara, Federico (Author) , Hofstede, Floris (Author) , Simon, Marleen E. H. (Author) , Jaarsveld, Richard H. van (Author) , Oegema, Renske (Author) , Gassen, Koen L. I. van (Author) , Holwerda, Sjoerd J. B. (Author) , Barakat, Tahsin Stefan (Author) , Bouman, Arjan (Author) , Slegtenhorst, Marjon van (Author) , Álvarez, Sara (Author) , Fernández-Jaén, Alberto (Author) , Porta, Javier (Author) , Accogli, Andrea (Author) , Mancardi, Margherita Maria (Author) , Striano, Pasquale (Author) , Iacomino, Michele (Author) , Chae, Jong-Hee (Author) , Jang, SeSong (Author) , Kim, Soo Y. (Author) , Chitayat, David (Author) , Mercimek-Andrews, Saadet (Author) , Depienne, Christel (Author) , Kampmeier, Antje (Author) , Kuechler, Alma (Author) , Surowy, Harald (Author) , Bertini, Enrico Silvio (Author) , Radio, Francesca Clementina (Author) , Mancini, Cecilia (Author) , Pizzi, Simone (Author) , Tartaglia, Marco (Author) , Gauthier, Lucas (Author) , Genevieve, David (Author) , Tharreau, Mylène (Author) , Azoulay, Noy (Author) , Zaks-Hoffer, Gal (Author) , Gilad, Nesia K. (Author) , Orenstein, Naama (Author) , Bernard, Geneviève (Author) , Thiffault, Isabelle (Author) , Denecke, Jonas (Author) , Herget, Theresia (Author) , Kortüm, Fanny (Author) , Kubisch, Christian (Author) , Bähring, Robert (Author) , Kindler, Stefan (Author) ,

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PHIP-associated Chung-Jansen syndrome: report of 23 new individuals by Kampmeier, Antje (Author) , Leitão, Elsa (Author) , Parenti, Ilaria (Author) , Beygo, Jasmin (Author) , Depienne, Christel (Author) , Bramswig, Nuria C (Author) , Hsieh, Tzung-Chien (Author) , Afenjar, Alexandra (Author) , Beck-Wödl, Stefanie (Author) , Grasshoff, Ute (Author) , Haack, Tobias B (Author) , Bijlsma, Emilia K (Author) , Ruivenkamp, Claudia (Author) , Lausberg, Eva (Author) , Elbracht, Miriam (Author) , Haanpää, Maria K (Author) , Koillinen, Hannele (Author) , Heinrich, Uwe (Author) , Rost, Imma (Author) , Jamra, Rami Abou (Author) , Popp, Denny (Author) , Koch-Hogrebe, Margarete (Author) , Rostasy, Kevin (Author) , López-González, Vanesa (Author) , Sanchez-Soler, María José (Author) , Macedo, Catarina (Author) , Schmetz, Ariane (Author) , Steinborn, Carmen (Author) , Weidensee, Sabine (Author) , Lesmann, Hellen (Author) , Marbach, Felix (Author) , Caro, Pilar (Author) , Schaaf, Christian P. (Author) , Krawitz, Peter (Author) , Wieczorek, Dagmar (Author) , Kaiser, Frank J (Author) , Kuechler, Alma (Author) ,

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Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with and Repeat Expansions: An 18-Year Study by Rosenbohm, Angela (Author) , Pott, Hendrik (Author) , Thomsen, Mirja (Author) , Rafehi, Haloom (Author) , Kaya, Sabine (Author) , Szymczak, Silke (Author) , Volk, Alexander E. (Author) , Mueller, Kathrin (Author) , Silveira, Isabel (Author) , Weishaupt, Jochen H. (Author) , Tönnies, Holger (Author) , Seibler, Philip (Author) , Zschiedrich, Katja (Author) , Schaake, Susen (Author) , Westenberger, Ana (Author) , Zühlke, Christine (Author) , Depienne, Christel (Author) , Trinh, Joanne (Author) , Ludolph, Albert C. (Author) , Klein, Christine (Author) , Bahlo, Melanie (Author) , Lohmann, Katja (Author) ,

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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction by Hoed, Joery den (Author) , de Boer, Elke (Author) , Voisin, Norine (Author) , Dingemans, Alexander J. M. (Author) , Guex, Nicolas (Author) , Wiel, Laurens (Author) , Nellaker, Christoffer (Author) , Amudhavalli, Shivarajan M. (Author) , Banka, Siddharth (Author) , Bena, Frederique S. (Author) , Ben-Zeev, Bruria (Author) , Bonagura, Vincent R. (Author) , Bruel, Ange-Line (Author) , Brunet, Theresa (Author) , Brunner, Han G. (Author) , Chew, Hui B. (Author) , Chrast, Jacqueline (Author) , Cimbalistienė, Loreta (Author) , Coon, Hilary (Author) , Délot, Emmanuèlle C. (Author) , Démurger, Florence (Author) , Denommé-Pichon, Anne-Sophie (Author) , Depienne, Christel (Author) , Donnai, Dian (Author) , Dyment, David A. (Author) , Elpeleg, Orly (Author) , Faivre, Laurence (Author) , Gilissen, Christian (Author) , Granger, Leslie (Author) , Haber, Benjamin (Author) , Hachiya, Yasuo (Author) , Abedi, Yasmin Hamzavi (Author) , Hanebeck, Jennifer (Author) , Hehir-Kwa, Jayne Y. (Author) , Horist, Brooke (Author) , Itai, Toshiyuki (Author) , Kotzaeridou, Urania (Author) , Orec, Laura (Author) ,

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A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes