Bibliographic Details
| Title: |
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language |
| Authors: |
Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance, Nowak, Catherine, Douglas, Jessica, Swoboda, Kathryn, Steeves, Marcie, Sahai, Inderneel, Stumpel, Connie, Stegmann, Alexander, Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William, Cohen, Ana, Agbahovbe, Ruky, Innes, A., Au, P., Rankin, Julia, Anderson, Ilse, Skinner, Steven, Louie, Raymond, Warren, Hannah, Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong, Price, Susan, Schnur, Rhonda, Douglas, Ganka, Wentzensen, Ingrid, Zweier, Christiane, Reis, André, Bialer, Martin, Moore, Christine, Koopmans, Marije, Brilstra, Eva, Monroe, Glen, Gassen, Koen, Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes, Wortmann, Saskia, Jakielski, Kathy, Strand, Edythe, Kloth, Katja, Bierhals, Tatjana, Roberts, John, Petrovich, Robert, Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han, Wade, Paul, Fisher, Simon, Campeau, Philippe |
| Source: |
Nature communications. 9(1):1-12 |
| Availability: |
http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100126212648.0x000001&indx=1&recIds=ETOCvdc_100126212648.0x000001 |
| Database: |
British Library Document Supply Centre Inside Serials & Conference Proceedings |
