E. Leenheer

Laterality and unilateral deafness: Patients with congenital right ear deafness do not develop atypical language dominance

G. Vingerhoets, M. Brysbaert, L. Haegen, 2016, Neuropsychologia.

DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System

Jason J. Corneveaux, M. Bitner-Glindzicz, G. Mortier, 2016, Human mutation.

Middle ear problems in children with cleft palate: A cross-sectional study

H. Hoecke, E. Leenheer, F. Dochy, 2019, Archives of Otolaryngology and Rhinology.

Stickler syndrome: comprehensive clinical and molecular analysis

G. Mortier, A. Paepe, I. Dhooge, 2016 .

Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).

C. Cremers, E. Leenheer, P. Huygen, 2001, Archives of otolaryngology--head & neck surgery.

Etiological diagnosis in the hearing impaired newborn: proposal of a flow chart.

S. Janssens, I. Dhooge, B. Leroy, 2011, International journal of pediatric otorhinolaryngology.