Sacred Heart University DigitalCommons@SHU Communication Disorders Faculty Publications Communication Disorders 11-2011 Genotype and Cardiovascular Phenotype Correlations With TBX1 in 1,022 Velo-Cardio-Facial/Digeorge/22q11.2 Deletion Syndrome Patients Tingwei Guo Donna McDonald-McGinn Anna Blonska Alan L. Shanske Anne S. Bassett See next page for additional authors Follow this and additional works at: https://digitalcommons.sacredheart.edu/speech_fac Part of the Communication Sciences and Disorders Commons, and the Congenital, Hereditary, and Neonatal Diseases and Abnormalities Commons Recommended Citation Guo,Tingwei, et al. "Genotype and Cardiovascular Phenotype Correlations With TBX1 in 1,022 Velo-Cardio- Facial/Digeorge/22q11.2 Deletion Syndrome Patients." Human Mutation 32.11 (2011): 1278-1289. This Peer-Reviewed Article is brought to you for free and open access by the Communication Disorders at DigitalCommons@SHU. It has been accepted for inclusion in Communication Disorders Faculty Publications by an authorized administrator of DigitalCommons@SHU. For more information, please contact
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[email protected]. Authors Tingwei Guo, Donna McDonald-McGinn, Anna Blonska, Alan L. Shanske, Anne S. Bassett, Eva Chow, Mark Bowser, Molly Sheridan, Frits Beemer, Koen Devriendt, Ann Swillen, Jeroen Breckpot, Maria C. Digilio, Bruno Marino, Bruno Dallapiccola, Courtney Carpenter, Xin Zheng, Jacob Johnson, Jonathan Chung, Anne Marie Higgins, Nicole Philip, Tony J. Simon, Karlene Coleman, Damian Heine-Suner, Jordi Rosell, Wendy R. Kates, Marcella Devoto, Elizabeth Goldmuntz, Elaine Zackai, Tao Wang, Robert J. Shprintzen, Beverly Emanuel, Bernice Morrow, and The International Chromosome 22q11.2 Consortium This peer-reviewed article is available at DigitalCommons@SHU: https://digitalcommons.sacredheart.edu/ speech_fac/82 NIH Public Access Author Manuscript Hum Mutat.