Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome

Por Palmer, Lisa, Butcher, Nancy J., Boot, Erik, Hodgkinson, Kathleen A., Heung, Tracy, Chow, Eva WC, Guna, Alina, Crowley, T. Blaine, Zackai, Elaine, McDonald-McGinn, Donna M., Bassett, Anne S.
Publicado no Am J Med Genet A (2018)

Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome

Por Bassett, Anne S., Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Chow, Eva W. C., van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E., Swillen, Ann, Van den Bree, Marianne, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E., Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Repetto, Gabriela M., Simon, Tony, Boot, Erik, Heung, Tracy, Evers, Rens, Vingerhoets, Claudia, van Duin, Esther, Zakai, Elaine, Vergaelen, Elfi, Devriendt, Koen, Vermeesch, Joris R., Owen, Michael, Murphy, Clodagh, Michaelovosky, Elena, Kushan, Leila, Schneider, Maude, Fremont, Wanda, Busa, Tiffany, Hooper, Stephen, McCabe, Kathryn, Duijff, Sasja, Isaev, Karin, Pellecchia, Giovanna, Wei, John, Gazzellone, Matthew J., Scherer, Stephen W., Emanuel, Beverly S., Guo, Tingwei, Morrow, Bernice E., Marshall, Christian R.
Publicado no Am J Psychiatry (2017)