Your search returned 2 results.

Results
	1.	A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21. [electronic resource] by Ismailov, S M Fedotov, V P Dadali, E L Polyakov, A V Van Broeckhoven, C Ivanov, V I De Jonghe, P Timmerman, V Evgrafov, O V Producer: 20010920 In: European journal of human genetics : EJHG vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients. [electronic resource] by Mersiyanova, I V Ismailov, S M Polyakov, A V Dadali, E L Fedotov, V P Nelis, E Löfgren, A Timmerman, V van Broeckhoven, C Evgrafov, O V Producer: 20000516 In: Human mutation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search