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Query Trace: Smith-Lemli-Opitz Syndrome and APOE[original query] |
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Maternal ABCA1 genotype is associated with severity of Smith-Lemli-Opitz syndrome and with viability of patients homozygous for null mutations. European journal of human genetics : EJHG 2012 Aug . Lanthaler B, Steichen-Gersdorf E, Kollerits B, Zschocke J, Witsch-Baumgartner M |
- Page last reviewed:Feb 1, 2024
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