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	1.	Three novel mutations of the NF1 gene detected by temperature gradient gel electrophoresis of exons 5 and 8. [electronic resource] by Horn, D Robinson, P N Böddrich, A Buske, A Tinschert, S Nürnberg, P Producer: 19970311 In: Electrophoresis vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Reduced neurofibromin content but normal GAP activity in a patient with neurofibromatosis type 1 caused by a five base pair duplication in exon 12b of the NF1 gene. [electronic resource] by Böddrich, A Griesser, J Horn, D Kaufmann, D Krone, W Nürnberg, P Producer: 19951102 In: Biochemical and biophysical research communications vol. 214 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	New evidence for a mutation hotspot in exon 37 of the NF1 gene. [electronic resource] by Böddrich, A Robinson, P N Schülke, M Buske, A Tinschert, S Nürnberg, P Producer: 19970626 In: Human mutation vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 gene. [electronic resource] by Robinson, P N Böddrich, A Peters, H Tinschert, S Buske, A Kaufmann, D Nürnberg, P Producer: 19950817 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia. [electronic resource] by Strom, T M Francis, F Lorenz, B Böddrich, A Econs, M J Lehrach, H Meitinger, T Producer: 19970827 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene. [electronic resource] by Lorenz, B Francis, F Gempel, K Böddrich, A Josten, M Schmahl, W Schmidt, J Lehrach, H Meitinger, T Strom, T M Producer: 19980416 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets. [electronic resource] by Francis, F Strom, T M Hennig, S Böddrich, A Lorenz, B Brandau, O Mohnike, K L Cagnoli, M Steffens, C Klages, S Borzym, K Pohl, T Oudet, C Econs, M J Rowe, P S Reinhardt, R Meitinger, T Lehrach, H Producer: 19970915 In: Genome research vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)