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	1.	Mutation analysis in Charcot-Marie-Tooth disease type 1 (CMT1). [electronic resource] by Sorour, E Upadhyaya, M Producer: 19990630 In: Human mutation vol. Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Brain drain: the issues raised for Egypt by the emigration of psychiatrists. [electronic resource] by Loza, N Sorour, E Publication details: BJPsych international Aug 2016 In: BJPsych international vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Novel mutation of the myelin P0 gene in a CMT1B family. [electronic resource] by Sorour, E MacMillan, J Upadhyaya, M Producer: 19970319 In: Human mutation vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Inheritance of CMT1A duplication from a mosaic father. [electronic resource] by Sorour, E Thompson, P MacMillan, J Upadhyaya, M Producer: 19951012 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A cytogenetic deletion, del(17)(q11.22q21.1), in a patient with sporadic neurofibromatosis type 1 (NF1) associated with dysmorphism and developmental delay. [electronic resource] by Upadhyaya, M Roberts, S H Maynard, J Sorour, E Thompson, P W Vaughan, M Wilkie, A O Hughes, H E Producer: 19970512 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)