Lang-Roth Ruth

A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus

C. Weiller, R. Lang-Roth, T. Deufel, 2001, European Journal of Human Genetics.

Extension of the clinical and molecular phenotype of DIAPH1‐associated autosomal dominant hearing loss (DFNA1)

U. Zimmermann, M. Knipper, H. Bolz, 2017, Clinical genetics.

Laryngeal electromyography: a proposal for guidelines of the European Laryngological Society

G. Friedrich, A. Mueller, C. Klingner, 2012, European Archives of Oto-Rhino-Laryngology.

Electrocochleography in children with auditory synaptopathy/neuropathy: diagnostic findings and characteristic parameters.

R. Lang-Roth, D. Beutner, M. Walger, 2015, International journal of pediatric otorhinolaryngology.

Prevalence and risk factors for hearing loss in high‐risk neonates in Germany

R. Lang-Roth, D. Beutner, B. Roth, 2019, Acta paediatrica.