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Dive into the research topics of 'Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia'. Together they form a unique fingerprint.- Sort by
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Margaret J. Wat, Oleg A. Shchelochkov, Ashley M. Holder, Amy M. Breman, Aditi Dagli, Carlos Bacino, Fernando Scaglia, Roberto T. Zori, Sau Wai Cheung, Daryl A. Scott, Sung Hae Lee Kang
Research output: Contribution to journal › Article › peer-review