Your search returned 4 results.

Results
	1.	INPP5K variant causes autosomal recessive congenital cataract in a Pakistani family. [electronic resource] by Yousaf, S Sheikh, S A Riazuddin, S Waryah, A M Ahmed, Z M Producer: 20190911 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15. [electronic resource] by Waryah, A M Rehman, A Ahmed, Z M Bashir, Z-H Khan, S Y Zafar, A U Riazuddin, S Friedman, T B Riazuddin, S Producer: 20100126 In: Clinical genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. [electronic resource] by Waryah, A M Shahzad, M Shaikh, H Sheikh, S A Channa, N A Hufnagel, R B Makhdoom, A Riazuddin, S Ahmed, Z M Producer: 20170522 In: Clinical genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mutations of human TMHS cause recessively inherited non-syndromic hearing loss. [electronic resource] by Shabbir, M I Ahmed, Z M Khan, S Y Riazuddin, Saima Waryah, A M Khan, S N Camps, R D Ghosh, M Kabra, M Belyantseva, I A Friedman, T B Riazuddin, Sheikh Producer: 20061227 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)