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Items where Author is "Binkert, Franz"

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Jump to: 2010 | 2009
Number of items: 2.

2010

Binkert, Franz and Spreiz, Ana and Höckner, Martina and Miny, Peter and von Dach Leu, Brigitte and Erdel, Martin and Zschocke, Johannes and Utermann, Gerd and Kotzot, Dieter. (2010) Parental origin and mechanism of formation of a 46,X,der(X)(pter--<q21.1::p11.4--<pter)/45,X karyotype in a woman with mild Turner syndrome. Fertility and sterility, Vol. 94, H. 1 , 350.e12-5.

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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