Items where Author is "Röthlisberger, B."
Jump to: Article Number of items: 3. ArticleFilges, I. and Röthlisberger, B. and Blattner, A. and Boesch, N. and Demougin, P. and Wenzel, F. and Huber, A. R. and Heinimann, K. and Weber, P. and Miny, P.. (2011) Deletion in Xp22.11 : PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism. Clinical genetics, Vol. 79, H. 1. pp. 79-85. Röthlisberger, B. and Huber, A. and Bargetzi, M. and Mendez, A. and Heizmann, M.. (2008) JAK2 exon 12 mutation in JAK2V617F-negative polycythemia vera. Leukemia & lymphoma, Vol. 49. pp. 586-588. Filges, I. and Röthlisberger, B. and Wenzel, F. and Heinimann, K. and Huber, A. R. and Miny, P.. (2008) Mosaic ring chromosome 8 : clinical and array-CGH findings in partial trisomy 8. American journal of medical genetics. Part A, Vol. 146, H. 21. pp. 2837-2841. |
