Eva J. J. Verver

A study of the clinical and radiological features in a cohort of 93 patients with a <i>COL2A1</i> mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype

Rutger Jan Nievelstein, Eva J. J. Verver, Vedat Topsakal et al. · American Journal of Medical Genetics Part A · 2015 · 94 citations · Full text

Short Stature, Genetics, Related Phenotype +22

Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2

Celia Zazo Seco, Luciana Serrão de Castro, Josephine W. van Nierop et al. · The American Journal of Human Genetics · 2015 · 73 citations · Full text

Encoding Kit Ligand, Allelic Variant, Mendelian Disorder +10

Ear and hearing problems in relation to karyotype in children with Turner syndrome

Eva J. J. Verver, Kim Freriks, Hans G. X. M. Thomeer et al. · Hearing Research · 2010 · 42 citations

Hearing Problems, Pediatric Otolaryngology, Audiology +4

Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease

Eva J. J. Verver, Vedat Topsakal, Henricus P. M. Kunst et al. · Ear and Hearing · 2015 · 36 citations

Cochlear implantation is safe and effective in patients with MYH9-related disease

Alessandro Pecci, Eva J. J. Verver, Nicole Schlegel et al. · Orphanet Journal of Rare Diseases · 2014 · 32 citations · Full text