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Dive into the research topics of 'Copy-number variation of the glucose transporter gene SLC2A3 and congenital heart defects in the 22q11.2 deletion syndrome'. Together they form a unique fingerprint.- Sort by
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Elisabeth E. Mlynarski, Molly B. Sheridan, Michael Xie, Tingwei Guo, Silvia E. Racedo, Donna M. McDonald-Mcginn, Xiaowu Gai, Eva W.C. Chow, Jacob Vorstman, Ann Swillen, Koen Devriendt, Jeroen Breckpot, Maria Cristina Digilio, Bruno Marino, Bruno Dallapiccola, Nicole Philip, Tony J. Simon, Amy E. Roberts, Małgorzata Piotrowicz, Carrie E. Bearden
Research output: Contribution to journal › Article › peer-review