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Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

by Fitzgerald, Tomas W, Kaplanis, Joanna, Aitken, Stuart, Jones, Philip, Singh, Tarjinder, Banka, Siddharth, Baralle, Diana, Barnicoat, Angela, Berg, Jonathan, Blair, Edward, Bohanna, David, Bourdon, Louise, Bourn, David, Bradley, Lisa, Brewer, Carole, Bunyan, David J, Chatzimichali, Elena, Clasper, Susan, Cole, Trevor, Colgiu, Irina, Collins, Amanda, Davidson, Rosemarie, Donaldson, Alan, Donnelly, Carina, Douglas, Angela, Douzgou, Sofia, Ellard, Sian, Ellis, Ian, Evans, Karenza, Everest, Sarah, Gardiner, Carol, Ghali, Neeti, Gibbons, Richard, Gill, Harinder, Goodship, Judith, Gray, Emma, Greene, Philip, Liu, He, Hellens, Stephen, Hildyard, Lucy, Holder, Muriel, Hutton, Ben, Ingram, Stuart, Irving, Melita, Josifova, Dragana, Joss, Shelagh, Kazembe, Sandra, Kerr, Bronwyn, Kingston, Helen, Kirby, Gail, Kirk, Claire, Kumar, Dhavendra, Vk Ajith Kumar, Lachlan, Katherine, Magee, Alex, Male, Alison, Mcconnell, Vivienne, Mckay, Kirsten, Mcmullan, Dominic J, Mcnerlan, Susan, Middleton, Anna, Miedzybrodzka, Zosia, Mohammed, Shehla, Morgan, Sian, Nemeth, Andrea, Parker, Michael J, Paterson, Joan, Perrett, Daniel, Pottinger, Caroline, Price, Sue, Ragge, Nicola, Rankin, Julia, Rice, Debbie, Samant, Shalaka, Schweiger, Susann, Scott, Richard, Selby, Ann, Seller, Anneke, Shears, Debbie, Sheridan, Eamonn, Smithson, Sarah, Splitt, Miranda, Squires, Miranda, Stewart, Fiona, Straub, Volker, Suri, Mohnish, Sutton, Vivienne, Thomson, Jenny, Tysoe, Carolyn, Wakeling, Emma, Whiteford, Margo, Widaa, Sara, Wilcox, Sarah, Wilkinson, Emily, Williams, Nicola, Yates, Laura, Firth, Helen V, Wright, Caroline F, Barrett, Jeffrey C, Hurles, Matthew E
Published in bioRxiv (16.06.2016)

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