Amanda Thum Welter

Report of the Phenotype of a Patient with Roberts Syndrome and a Rare ESCO2 Variant.

U. Francke, B. Schüle, M. Fiegenbaum, 2019, Journal of pediatric genetics.

Trisomy 21 and Ebstein Anomaly: Diagnosis and Prognosis of a Rare Association

R. Rosa, P. Zen, Amanda Thum Welter, 2020, Journal of Pediatric Genetics.