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HARVARD Citation
Temple, S. et al. (2020). Familial DHCR7 genotype presenting as a very mild form of Smith‐Lemli‐Opitz syndrome and lethal holoprosencephaly. JIMD reports. 56 (1), pp. 3-8. [Online].
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Temple, S. et al. (2020). Familial DHCR7 genotype presenting as a very mild form of Smith‐Lemli‐Opitz syndrome and lethal holoprosencephaly. JIMD reports. 56 (1), pp. 3-8. [Online].