Rikkert L. Snoeckx

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 551 citations · Full text

Genetic Disorder, Genetics, Audiology +9

A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene

Guy Van Camp, Rikkert L. Snoeckx, Nele Hilgert et al. · The American Journal of Human Genetics · 2006 · 181 citations · Full text

Stickler Syndrome Is, Autoimmune Disease, Mendelian Disorder +10

Mutation analysis of the GJB2 (Connexin 26) gene in Egypt

Rikkert L. Snoeckx, Dalia Hassan, Nadia Kamal et al. · Human Mutation · 2005 · 72 citations · Full text

A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3

Rikkert L. Snoeckx · Journal of Medical Genetics · 2004 · 23 citations · Full text

<i>GJB2</i> (connexin 26) mutations are not a major cause of hearing loss in the Indonesian population

Rikkert L. Snoeckx, Bulantrisna Djelantik, Lut Van Laer et al. · American Journal of Medical Genetics Part A · 2005 · 17 citations