Lanthaler, B., Steichen-Gersdorf, E., Kollerits, B., Zschocke, J., & Witsch-Baumgartner, M. (2013). Maternal ABCA1 genotype is associated with severity of Smith–Lemli–Opitz syndrome and with viability of patients homozygous for null mutations. Nature Publishing Group.

Lanthaler, Barbara, Elisabeth Steichen-Gersdorf, Barbara Kollerits, Johannes Zschocke, and Martina Witsch-Baumgartner. Maternal ABCA1 Genotype Is Associated With Severity of Smith–Lemli–Opitz Syndrome and With Viability of Patients Homozygous for Null Mutations. Nature Publishing Group, 2013.

Lanthaler, Barbara, et al. Maternal ABCA1 Genotype Is Associated With Severity of Smith–Lemli–Opitz Syndrome and With Viability of Patients Homozygous for Null Mutations. Nature Publishing Group, 2013.