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Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern.
Schoner K, Witsch-Baumgartner M, Behunova J, Petrovic R, Bald R, Kircher SG, Ramaswamy A, Kluge B, Meyer-Wittkopf M, Schmitz R, Fritz B, Zschocke J, Laccone F, Rehder H. Schoner K, et al. Among authors: kluge b. Birth Defects Res. 2020 Jan 15;112(2):175-185. doi: 10.1002/bdr2.1620. Epub 2019 Dec 16. Birth Defects Res. 2020. PMID: 31840946 Free PMC article.
Variations of frataxin protein levels in normal individuals.
Boehm T, Scheiber-Mojdehkar B, Kluge B, Goldenberg H, Laccone F, Sturm B. Boehm T, et al. Among authors: kluge b. Neurol Sci. 2011 Apr;32(2):327-30. doi: 10.1007/s10072-010-0326-1. Epub 2010 May 27. Neurol Sci. 2011. PMID: 20506029
38 results