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Dive into the research topics of 'Mutations in the human sterol Δ7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome'. Together they form a unique fingerprint.- Sort by
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Christopher A. Wassif, Cheryl Maslen, Stivelia Kachilele-Linjewile, Don Lin, Leesa M. Linck, William E. Connor, Robert D. Steiner, Forbes D. Porter
Research output: Contribution to journal › Article › peer-review