Search Results - "Kupsch, Petra" :: K.UTB vyhledávací portál

Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population

by Gabriel, Heinz, Kupsch, Petra, Sudendey, Jürgen, Winterhager, Elke, Jahnke, Klaus, Lautermann, Jürgen
Published in Human mutation (01.06.2001)

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$Results of a Phase I Trial of Sorafenib (BAY 43-9006) in Combination with Oxaliplatin in Patients with Refractory Solid Tumors, Including Colorectal Cancer$

Results of a Phase I Trial of Sorafenib (BAY 43-9006) in Combination with Oxaliplatin in Patients with Refractory Solid Tumors, Including Colorectal Cancer

by Kupsch, Petra, Henning, Bernhard F., Passarge, Katrin, Richly, Heike, Wiesemann, Katrin, Hilger, Ralf A., Scheulen, Max E., Christensen, Olaf, Brendel, Erich, Schwartz, Brian, Hofstra, Elke, Voigtmann, Rudolf, Seeber, Siegfried, Strumberg, Dirk
Published in Clinical colorectal cancer (01.09.2005)

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Journal Article

Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population

Results of a Phase I Trial of Sorafenib (BAY 43-9006) in Combination with Oxaliplatin in Patients with Refractory Solid Tumors, Including Colorectal Cancer

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