Items where Author is "Miny, P."

2013

De Geyter, C. and Sterthaus, O. and Miny, P. and Wenzel, F. and Lapaire, O. and De Geyter, M. and Sartorius, G.. (2013) First successful pregnancy in Switzerland after prospective sex determination of the embryo through the separation of X-chromosome bearing spermatozoa. Swiss medical weekly, Vol. 143 , w13718.

Heng, B. C. and Heinimann, K. and Miny, P. and Iezzi, G. and Glatz, K. and Scherberich, A. and Zulewski, H. and Fussenegger, M.. (2013) mRNA transfection-based, feeder-free, induced pluripotent stem cells derived from adipose tissue of a 50-year-old patient. Metabolic Engineering, 18. pp. 9-24.

2011

Filges, 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.

2010

van Kuilenburg, A. B. P. and Meijer, J. and Gökcay, G. and Baykal, T. and Rubio-Gozalbo, M. E. and Mul, A. N. P. M. and de Die-Smulders, C. E. M. and Weber, P. and Mori, A. Capone and Bierau, J. and Fowler, B. and Macke, K. and Sass, J. O. and Meinsma, R. and Hennermann, J. B. and Miny, P. and Zoetekouw, L. and Roelofsen, J. and Vijzelaar, R. and Nicolai, J. and Hennekam, R. C. M.. (2010) Dihydropyrimidine dehydrogenase deficiency caused by a novel genomic deletion c.505_513del of DPYD. Nucleosides, nucleotides & nucleic acids, Vol. 29, H. 4-6. pp. 509-514.

2009

Siitonen, H. A. and Sotkasiira, J. and Biervliet, M. and Benmansour, A. and Capri, Y. and Cormier-Daire, V. and Crandall, B. and Hannula-Jouppi, K. and Hennekam, R. and Herzog, D. and Keymolen, K. and Lipsanen-Nyman, M. and Miny, P. and Plon, S. E. and Riedl, S. and Sarkar, A. and Vargas, F. R. and Verloes, A. and Wang, L. L. and Kääriäinen, H. and Kestilä, M.. (2009) The mutation spectrum in RECQL4 diseases. European journal of human genetics : EJHG : the official journal of the European Society of Human Genetics, Vol. 17. pp. 151-158.

2008

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.