Florian Marsch

Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula

D. Tibboel, M. Lacher, P. Hoffmann, 2016, European Journal of Human Genetics.

Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?

J. Altmüller, H. Thiele, H. Reutter, 2017, Molecular medicine reports.

Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs

U. Gembruch, H. Reutter, M. Ludwig, 2016, Journal of Neurodevelopmental Disorders.

CNV analysis in 169 patients with bladder exstrophy-epispadias complex

M. Nöthen, S. Moebus, A. Brusco, 2016, BMC Medical Genetics.

Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs

A. Hofmann, U. Gembruch, H. Reutter, 2016, Journal of Neurodevelopmental Disorders.

Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.

S. Heilmann-Heimbach, M. Lacher, F. Degenhardt, 2017, Birth defects research.