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	1.	Cracking the auditory genetic code: nonsyndromic hereditary hearing impairment. [electronic resource] by Lalwani, A K Castelein, C M Producer: 19990322 In: The American journal of otology vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	2.	A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration. [electronic resource] by Lalwani, A K Luxford, W M Mhatre, A N Attaie, A Wilcox, E R Castelein, C M Producer: 19990310 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9. [electronic resource] by Lalwani, A K Goldstein, J A Kelley, M J Luxford, W Castelein, C M Mhatre, A N Producer: 20001214 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)
	4.	Dominant modifier DFNM1 suppresses recessive deafness DFNB26. [electronic resource] by Riazuddin, S Castelein, C M Ahmed, Z M Lalwani, A K Mastroianni, M A Naz, S Smith, T N Liburd, N A Friedman, T B Griffith, A J Riazuddin, S Wilcox, E R Producer: 20010104 In: Nature genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)