Search Results - Thiffault, Isabelle
- Showing 1 - 2 results of 2
-
1
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) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource -
2
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome by Tessadori, Federico (Author) , Duran, Karen (Author) , Knapp, Karen (Author) , Fellner, Matthias (Author) , Smithson, Sarah (Author) , Beleza Meireles, Ana (Author) , Elting, Mariet W. (Author) , Waisfisz, Quinten (Author) , O’Donnell-Luria, Anne (Author) , Nowak, Catherine (Author) , Douglas, Jessica (Author) , Ronan, Anne (Author) , Brunet, Theresa (Author) , Kotzaeridou, Urania (Author) , Svihovec, Shayna (Author) , Saenz, Margarita S. (Author) , Thiffault, Isabelle (Author) , Del Viso, Florencia (Author) , Devine, Patrick (Author) , Rego, Shannon (Author) , Tenney, Jessica (Author) , van Haeringen, Arie (Author) , Ruivenkamp, Claudia A. L. (Author) , Koene, Saskia (Author) , Robertson, Stephen P. (Author) , Deshpande, Charulata (Author) , Pfundt, Rolph (Author) , Verbeek, Nienke (Author) , van de Kamp, Jiddeke M. (Author) , Weiss, Janneke M. M. (Author) , Ruiz, Anna (Author) , Gabau, Elisabeth (Author) , Banne, Ehud (Author) , Pepler, Alexander (Author) , Bottani, Armand (Author) , Laurent, Sacha (Author) , Guipponi, Michel (Author) , Bijlsma, Emilia (Author) , Bruel, Ange-Line (Author) , Sorlin, Arthur (Author) , Willis, Mary (Author) , Powis, Zoe (Author) , Smol, Thomas (Author) , Vincent-Delorme, Catherine (Author) , Baralle, Diana (Author) , Colin, Estelle (Author) , Revencu, Nicole (Author) , Calpena, Eduardo (Author) , Wilkie, Andrew O. M. (Author) , Chopra, Maya (Author) , Cormier-Daire, Valerie (Author) , Keren, Boris (Author) , Afenjar, Alexandra (Author) , Niceta, Marcello (Author) , Terracciano, Alessandra (Author) , Specchio, Nicola (Author) , Tartaglia, Marco (Author) , Rio, Marlene (Author) , Barcia, Giulia (Author) , Rondeau, Sophie (Author) , Colson, Cindy (Author) , Bakkers, Jeroen (Author) , Mace, Peter D. (Author) , Bicknell, Louise S. (Author) , van Haaften, Gijs (Author) ,
Call Number: Loading…
Located: Loading…
Article (Journal) Online Resource