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Items where Author is "Röthlisberger, Benno"

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Jump to: 2011 | 2010 | 2009
Number of items: 4.

2011

Filges, Isabel and Shimojima, Keiko and Okamoto, Nobuhiko and Röthlisberger, Benno and Weber, Peter and Huber, Andreas R. and Nishizawa, Tsutomu and Datta, Alexandre N. and Miny, Peter and Yamamoto, Toshiyuki. (2011) Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndrome. Journal of medical genetics, Vol. 48, H. 2. pp. 117-122.

2010

Filges, Isabel and Röthlisberger, Benno and Boesch, Nemya and Weber, Peter and Wenzel, Friedel and Huber, Andreas R. and Heinimann, Karl and Miny, Peter. (2010) Interstitial deletion 1q42 in a patient with agenesis of corpus callosum : Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome. American journal of medical genetics. Part A, Vol. 152, H. 4. pp. 987-993.

Vogler, Christian and Gschwind, Leo and Röthlisberger, Benno and Huber, Andreas and Filges, Isabel and Miny, Peter and Auschra, Bianca and Stetak, Attila and Demougin, Philippe and Vukojevic, Vanja and Kolassa, Iris-Tatjana and Elbert, Thomas and de Quervain, Dominique J.-F. and Papassotiropoulos, Andreas. (2010) Microarray-based maps of copy-number variant regions in European and sub-saharan populations. PLoS ONE, 5 (12). e15246.

2009

Filges, Isabel and Röthlisberger, Benno and Noppen, Christoph and Boesch, Nemya and Wenzel, Friedel and Necker, Judith and Binkert, Franz and Huber, Andreas R. and Heinimann, Karl and Miny, Peter. (2009) Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33 : clinical and array-CGH study of a benign phenotype in a three-generation family. American journal of medical genetics, Vol. 149. pp. 237-241.

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