Concepedia

Rikkert L. Snoeckx

RL

Statistics

Publications

5

Citations

853

H-Index

5

Active since

2004

Affiliations

University of Antwerp(Current)

Antwerp University Hospital

Rikkert L. Snoeckx is an author at University of Antwerp specializing in genetic disorders, human genetics, and genetics.

Publications per year

2004–2006

5

Publications

5

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 · 559 citations · Full text

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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 · 182 citations · Full text

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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

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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

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<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

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