Kalb, S., & Hinderhofer, K. (2012). High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey. Clinical genetics, 81(6), . https://doi.org/10.1111/j.1399-0004.2011.01750.x
Chicago Style (17th ed.) CitationKalb, Stefanie, and Katrin Hinderhofer. "High Frequency of P.Thr93Met in Smith-Lemli-Opitz Syndrome Patients in Turkey." Clinical Genetics 81, no. 6 (2012). https://doi.org/10.1111/j.1399-0004.2011.01750.x.
MLA (9th ed.) CitationKalb, Stefanie, and Katrin Hinderhofer. "High Frequency of P.Thr93Met in Smith-Lemli-Opitz Syndrome Patients in Turkey." Clinical Genetics, vol. 81, no. 6, 2012, https://doi.org/10.1111/j.1399-0004.2011.01750.x.
Warning: These citations may not always be 100% accurate.