C. Samanns

Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa

Susanna Bunge, Heike Wedemann, D. David et al. · Genomics · 1993 · 121 citations · Full text

Genetics, Molecular Analysis, Molecular Biology +4

[Autosomal dominant hereditary retinopathia pigmentosa with genetic heterogeneity].

Ulrike Orth, C. Samanns, H Gusseck et al. · PubMed · 1991 · 40 citations

Mendelian Disorder, Point Mutations, Ophthalmology +15

Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type

Arthur A. Bergen, C. Samanns, E. J. M. Schuurman et al. · Human Genetics · 1991 · 35 citations

Ocular Disease, Ophthalmology, Multipoint Linkage Analysis +3

Gene for non‐specific X‐linked mental retardation maps in the pericentromeric region

C. Samanns, Regine Albrecht, M. Neugebauer et al. · American Journal of Medical Genetics · 1991 · 27 citations

Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis

Arthur A. Bergen, C. Samanns, D. B. van Dorp et al. · Ophthalmic Paediatrics and Genetics · 1990 · 17 citations