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Dive into the research topics of 'Carrier frequency of the common mutation IVS8-1G>C in DHCR7 and estimate of the expected incidence of Smith-Lemli-Opitz syndrome'. Together they form a unique fingerprint.- Sort by
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Kevin P. Battaile, Brian C. Battaile, Louise S. Merkens, Cheryl L. Maslen, Robert D. Steiner
Research output: Contribution to journal › Article › peer-review