K. Keppler

Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families.

M. Lacher, J. Schumacher, N. Zwink, 2016, Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus.

Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.

M. Nöthen, M. Lacher, N. Zwink, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing

A. Hoischen, M. Nöthen, C. Gilissen, 2017, Journal of dental research.

Genome‐wide CNV analysis in 221 unrelated patients and targeted high‐throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis

M. Nöthen, H. Fröhlich, S. Moebus, 2015, International journal of cancer.