Barbara Günther

<i>GJB2</i> mutations in keratitis‐ichthyosis‐deafness syndrome including its fatal form

Andreas Janecke, Hans Christian Hennies, Barbara Günther et al. · American Journal of Medical Genetics Part A · 2005 · 92 citations

Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

Pawaree Saisawat, Velibor Tasić, Virginia Vega-Warner et al. · Kidney International · 2011 · 85 citations · Full text

Sensorineural hearing loss and the incidence of Cx26 mutations in Austria

Judith Löffler, Doris Nekahm, Almut Hirst-Stadlmann et al. · European Journal of Human Genetics · 2001 · 84 citations · Full text

Sensorineural Hearing Loss, Cx26 Mutations, Audiology +5

Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria

Andreas Janecke, Almut Hirst-Stadlmann, Barbara Günther et al. · Human Genetics · 2002 · 74 citations

Genetic Disorder, Genetics, Audiology +10

The 342-kb deletion in<i>GJB6</i>is not present in patients with non-syndromic hearing loss from Austria

Barbara Günther, Andrea K. Steiner, Doris Nekahm-Heis et al. · Human Mutation · 2003 · 38 citations · Full text

342-Kb Deletion, Non-syndromic Hearing Loss, Mendelian Disorder +14