A method for accurate detection of genomic microdeletions using real-time quantitative PCR

por Weksberg, Rosanna, Hughes, Simon, Moldovan, Laura, Bassett, Anne S, Chow, Eva WC, Squire, Jeremy A
Publicado 2005

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

por Bassett, Anne S., Marshall, Christian R., Lionel, Anath C., Chow, Eva W.C., Scherer, Stephen W.
Publicado 2008

22q11.2 microdeletion and increased risk for type 2 diabetes

por Van, Lily, Heung, Tracy, Malecki, Sarah L., Fenn, Christian, Tyrer, Andrea, Sanches, Marcos, Chow, Eva W.C., Boot, Erik, Corral, Maria, Dash, Satya, George, Susan R., Bassett, Anne S.
Publicado 2020

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

por Guo, Tingwei, Repetto, Gabriela M., McDonald McGinn, Donna M., Chung, Jonathan H., Nomaru, Hiroko, Campbell, Christopher L., Blonska, Anna, Bassett, Anne S., Chow, Eva W.C., Mlynarski, Elisabeth E., Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E., Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E., Digilio, M. Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E., Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E., Tassone, Flora, Simon, Tony J., van Duin, Esther D.A., van Amelsvoort, Thérèse A., Kates, Wendy R., Zackai, Elaine, Johnston, H. Richard, Cutler, David J., Agopian, A.J., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Emanuel, Beverly S., Morrow, Bernice E.
Publicado 2017