Search Results - Winkelmann, Martina

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome by Rao, Ercole (Author) , Weiß, Birgit (Author) , Fukami, Maki (Author) , Rump, Andreas (Author) , Niesler, Beate (Author) , Mertz, Annelyse (Author) , Muroya, Koji (Author) , Binder, Gerhard (Author) , Kirsch, Stefan (Author) , Winkelmann, Martina (Author) , Nordsiek, Gabriele (Author) , Heinrich, Udo (Author) , Breuning, Martijn H. (Author) , Ranke, Michael B. (Author) , Rosenthal, André (Author) , Ogata, Tsutomu (Author) , Rappold, Gudrun (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of All (Y+)XX males and (Y-)XY females by Schiebel, Katrin (Author) , Winkelmann, Martina (Author) , Mertz, Annelyse (Author) , Xu, Xiaoling (Author) , Page, David C. (Author) , Weil, Dominique (Author) , Petit, Christine (Author) , Rappold, Gudrun (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability by Klink, Albrecht (Author) , Schiebel, Katrin (Author) , Winkelmann, Martina (Author) , Rao, Ercole (Author) , Horsthemke, Bernhard (Author) , Lüdecke, Hermann-Josef (Author) , Claussen, Uwe (Author) , Scherer, Gerd (Author) , Rappold, Gudrun (Author) ,

• Verlag, lizenzpflichtig, Volltext

Localization of the adenine nucleotide translocase gene ANT2 to chromosome Xq24-q25 with tight linkage to DXS425 by Schiebel, Katrin (Author) , Mertz, Annelyse (Author) , Winkelmann, Martina (Author) , Nagaraja, Ramaiah (Author) , Rappold, Gudrun (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext