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3 risultati 1
Postprint
Consortium of Swiss Academic Libraries

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

Bruder, Carl E.G. ; Hirvelä, Carina ; Tapia-Paez, Isabel ; Fransson, Ingegerd ; Segraves, Richard ; Hamilton, Greg ; Zhang, Xiao Xiao ; Evans, D. Gareth ; Wallace, Andrew J. ; Baser, Michael E. ; Zucman-Rossi, Jessica ; Hergersberg, Martin ; Boltshauser, Eugene ; Papi, Laura ; Rouleau, Guy A. ; Poptodorov, George ; Jordanova, Albena ; Rask-Andersen, Helge ; Kluwe, Lan ; Mautner, Victor ; Sainio, Markku ; Hung, Gene ; Mathiesen, Tiit ; Möller, Claes ; Pulst, Stefan M. ; Harder, Henrik ; Heiberg, Arvid ; Honda, Mariko ; Niimura, Michihito ; Sahlén, Sigrid ; Blennow, Elisabeth ; Albertson, Donna G. ; Pinkel, Daniel ; Dumanski, Jan P.

In: Human Molecular Genetics, 2001, vol. 10, no. 3, p. 271-282

Postprint
Consortium of Swiss Academic Libraries

Tissue-specific expression of a FMR1/β-galactosidase fusion gene in transgenic mice

Hergersberg, Martin ; Matsuo, Koichi ; Gassmann, Max ; Schaffner, Walter ; Lüscher, Bernhard ; Rülicke, Thomas ; Aguzzi, Adriano

In: Human Molecular Genetics, 1995, vol. 4, no. 3, p. 359-366

Postprint
Consortium of Swiss Academic Libraries

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

Kotzot, Dieter ; Schmitt, Silke ; Bernasconi, Fabiana ; Robinson, Wendy P. ; Lurie, Iosif W. ; Ilyina, Helena ; Méhes, Károly ; Hamel, Ben C.J. ; Otten, Barto J. ; Hergersberg, Martin ; Werder, Edmond ; Schoenle, Eugen ; Schinzel, Albert

In: Human Molecular Genetics, 1995, vol. 4, no. 4, p. 583-587

3 risultati 1