Your search returned 3 results.

Results
	1.	Improvement of the diagnostic procedure in proximal myotonic myopathy/myotonic dystrophy type 2. [electronic resource] by Jakubiczka, Sibylle Vielhaber, Stefan Kress, Wolfram Küpferling, Peter Reuner, Ulrike Kunath, Bernhard Wieacker, Peter Producer: 20040517 In: Neurogenetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations. [electronic resource] by Yue, Ying Farcas, Ruxandra Thiel, Gundula Bommer, Christiane Grossmann, Bärbel Galetzka, Danuta Kelbova, Christina Küpferling, Peter Daser, Angelika Zechner, Ulrich Haaf, Thomas Producer: 20070619 In: European journal of human genetics : EJHG vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature. [electronic resource] by Manvelyan, Marina Riegel, Mariluce Santos, Monica Fuster, Carme Pellestor, Franck Mazaurik, Marie-Luise Schulze, Bernt Polityko, Anna Tittelbach, Hanne Reising-Ackermann, Gisela Belitz, Britta Hehr, Ute Kelbova, Christina Volleth, Marianne Gödde, Elisabeth Anderson, Jasen Küpferling, Peter Köhler, Sigrid Duba, Hans-Christoph Dufke, Andreas Aktas, Dilek Martin, Thomas Schreyer, Isolde Ewers, Elisabeth Reich, Daniela Mrasek, Kristin Weise, Anja Liehr, Thomas Producer: 20080723 In: International journal of molecular medicine vol. 21 Availability: No items available. Save to lists Add to cart (remove)