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	1.	Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations. [electronic resource] by Amir, R E Zoghbi, H Y Producer: 20010628 In: American journal of medical genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms. [electronic resource] by Buyse, I M Fang, P Hoon, K T Amir, R E Zoghbi, H Y Roa, B B Producer: 20010118 In: American journal of human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. [electronic resource] by Amir, R E Van den Veyver, I B Wan, M Tran, C Q Francke, U Zoghbi, H Y Producer: 19991019 In: Nature genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Acute incremental exercise to maximal performance does not cause alterations in serum oxidant levels of healthy young individuals. [electronic resource] by Amir, O Yamin, C Sagiv, M Eynon, N Shnizer, S Kagan, T Reznick, A Z Sagiv, M Amir, R E Producer: 20090716 In: The Journal of sports medicine and physical fitness vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. [electronic resource] by Amir, R E Fang, P Yu, Z Glaze, D G Percy, A K Zoghbi, H Y Roa, B B Van den Veyver, I B Producer: 20060420 In: Journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots. [electronic resource] by Wan, M Lee, S S Zhang, X Houwink-Manville, I Song, H R Amir, R E Budden, S Naidu, S Pereira, J L Lo, I F Zoghbi, H Y Schanen, N C Francke, U Producer: 20000127 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. [electronic resource] by Amir, R E Van den Veyver, I B Schultz, R Malicki, D M Tran, C Q Dahle, E J Philippi, A Timar, L Percy, A K Motil, K J Lichtarge, O Smith, E O Glaze, D G Zoghbi, H Y Producer: 20000531 In: Annals of neurology vol. 47 Availability: No items available. Save to lists Add to cart (remove)