Human Genome Epidemiology Literature Finder
Records 1 - 1 (of 1 Records) |
Query Trace: Smith-Lemli-Opitz Syndrome and ABCA1[original query] |
---|
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:Oct 1, 2023
- Page last updated:Dec 11, 2023
- Content source: