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Dive into the research topics of 'Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations'. Together they form a unique fingerprint.- Sort by
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Brian J. O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J. Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P. MacKenzie, Sarah B. Ng, Carl Baker, Mark J. Rieder, Deborah A. Nickerson, Raphael Bernier, Simon E. Fisher, Jay Shendure, Evan E. Eichler
Research output: Contribution to journal › Article › peer-review