Search Results - Klink, Albrecht
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Pulsed-Field gel electrophoresis: protocols by Rappold, Gudrun (Author) , Ried, Karin (Author) , Klink, Albrecht (Author) , Rao, Ercole (Author) , Weiß, Birgit (Author) ,
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2
Refinement of the locus for X-linked recessive chondrodysplasia punctata by Muroya, Koji (Author) , Ogata, Tsutomu (Author) , Rappold, Gudrun (Author) , Klink, Albrecht (Author) , Nakahori, Yutaka (Author) , Fukushima, Yoshimitsu (Author) , Aizu, Katsuya (Author) , Matsuo, Nobutake (Author) ,
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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) ,
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Double crossover in the human Xp/Yp pseudoautosomal region and its bearing on interference by Rappold, Gudrun (Author) , Klink, Albrecht (Author) , Weiß, Birgit (Author) , Fischer, Christine (Author) ,
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A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval by Klink, Albrecht (Author) , Meindl, Alfons (Author) , Hellebrand, Heide (Author) , Rappold, Gudrun (Author) ,
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AK1 detects a VNTR locus in the pseudoautosomal region by Klink, Albrecht (Author) , Wapenaar, Martin C. (Author) , Ommen, G.J.B. van (Author) , Rappold, Gudrun (Author) ,
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