APA

Guo T., McDonald-McGinn D., Blonska A., Shanske A., Bassett A. S., Chow E., Bowser M., Sheridan M., Beemer F., Devriendt K., Swillen A., Breckpot J., Digilio M. C., Marino B., Dallapiccola B., Carpenter C., Zheng X., Johnson J., Chung J., Higgins A. M., Philip N., Simon T. J., Coleman K., Heine-Suner D., Rosell J., Kates W., Devoto M., Goldmuntz E., Zackai E., Wang T., Shprintzen R., Emanuel B. & Morrow B. (20120531). Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. : Human mutation.

Chicago

Guo Tingwei, McDonald-McGinn Donna, Blonska Anna, Shanske Alan, Bassett Anne S, Chow Eva, Bowser Mark, Sheridan Molly, Beemer Frits, Devriendt Koen, Swillen Ann, Breckpot Jeroen, Digilio Maria C, Marino Bruno, Dallapiccola Bruno, Carpenter Courtney, Zheng Xin, Johnson Jacob, Chung Jonathan, Higgins Anne Marie, Philip Nicole, Simon Tony J, Coleman Karlene, Heine-Suner Damian, Rosell Jordi, Kates Wendy, Devoto Marcella, Goldmuntz Elizabeth, Zackai Elaine, Wang Tao, Shprintzen Robert, Emanuel Beverly and Morrow Bernice. 20120531. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. : Human mutation.

Harvard

Guo T., McDonald-McGinn D., Blonska A., Shanske A., Bassett A. S., Chow E., Bowser M., Sheridan M., Beemer F., Devriendt K., Swillen A., Breckpot J., Digilio M. C., Marino B., Dallapiccola B., Carpenter C., Zheng X., Johnson J., Chung J., Higgins A. M., Philip N., Simon T. J., Coleman K., Heine-Suner D., Rosell J., Kates W., Devoto M., Goldmuntz E., Zackai E., Wang T., Shprintzen R., Emanuel B. and Morrow B. (20120531). Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. : Human mutation.

MLA

Guo Tingwei, McDonald-McGinn Donna, Blonska Anna, Shanske Alan, Bassett Anne S, Chow Eva, Bowser Mark, Sheridan Molly, Beemer Frits, Devriendt Koen, Swillen Ann, Breckpot Jeroen, Digilio Maria C, Marino Bruno, Dallapiccola Bruno, Carpenter Courtney, Zheng Xin, Johnson Jacob, Chung Jonathan, Higgins Anne Marie, Philip Nicole, Simon Tony J, Coleman Karlene, Heine-Suner Damian, Rosell Jordi, Kates Wendy, Devoto Marcella, Goldmuntz Elizabeth, Zackai Elaine, Wang Tao, Shprintzen Robert, Emanuel Beverly and Morrow Bernice. Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. : Human mutation. 20120531.