S. Herold

Rapid detection of subtelomeric deletion/duplication by novel real‐time quantitative PCR using SYBR‐green dye

Thomas Liehr, T. Liehr, A. Kuechler, 2004, Human mutation.

A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome

H. Rehder, P. Burfeind, B. Auber, 2007, Clinical genetics.

Adjustment formulae for maternal serum alpha‐fetoprotein, human chorionic gonadotropin, and unconjugated oestriol to maternal weight and smoking

I. Bartels, J. Caesar, B. Bockel, 1993, Prenatal diagnosis.

Prenatal diagnosis of a large de novo terminal deletion of chromosome 11q

B. Zoll, P. Burfeind, H. Pauer, 2006, Prenatal diagnosis.