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	1.	Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA). [electronic resource] by Prasad, S Cucci, R A Green, G E Smith, R J Producer: 20010111 In: Human mutation vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The M34T allele variant of connexin 26. [electronic resource] by Cucci, R A Prasad, S Kelley, P M Green, G E Storm, K Willocx, S Cohn, E S Van Camp, G Smith, R J Producer: 20010329 In: Genetic testing vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations. [electronic resource] by Campbell, C Cucci, R A Prasad, S Green, G E Edeal, J B Galer, C E Karniski, L P Sheffield, V C Smith, R J Producer: 20010830 In: Human mutation vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment. [electronic resource] by Van Laer, L Coucke, P Mueller, R F Caethoven, G Flothmann, K Prasad, S D Chamberlin, G P Houseman, M Taylor, G R Van de Heyning, C M Fransen, E Rowland, J Cucci, R A Smith, R J Van Camp, G Producer: 20011205 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A genotype-phenotype correlation for GJB2 (connexin 26) deafness. [electronic resource] by Cryns, K Orzan, E Murgia, A Huygen, P L M Moreno, F del Castillo, I Chamberlin, G Parker Azaiez, H Prasad, S Cucci, R A Leonardi, E Snoeckx, R L Govaerts, P J Van de Heyning, P H Van de Heyning, C M Smith, R J H Van Camp, G Producer: 20040615 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)