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	61.	Structure of the human paralemmin gene (PALM), mapping to human chromosome 19p13.3 and mouse chromosome 10, and exclusion of coding mutations in grizzled, mocha, jittery, and hesitant mice. [electronic resource] by Burwinkel, B Miglierini, G Jenne, D E Gilbert, D J Copeland, N G Jenkins, N A Ring, H Z Francke, U Kilimann, M W Producer: 19980803 In: Genomics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Mutation analysis in myophosphorylase deficiency (McArdle's disease). [electronic resource] by Vorgerd, M Kubisch, C Burwinkel, B Reichmann, H Mortier, W Tettenborn, B Pongratz, D Lindemuth, R Tegenthoff, M Malin, J P Kilimann, M W Producer: 19980410 In: Annals of neurology vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	The synaptic vesicle-associated protein amphiphysin is the 128-kD autoantigen of Stiff-Man syndrome with breast cancer. [electronic resource] by De Camilli, P Thomas, A Cofiell, R Folli, F Lichte, B Piccolo, G Meinck, H M Austoni, M Fassetta, G Bottazzo, G Bates, D Cartlidge, N Solimena, M Kilimann, M W Producer: 19931228 In: The Journal of experimental medicine vol. 178 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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