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	61.	SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis. [electronic resource] by Anwar, Saima Riazuddin, Saima Ahmed, Zubair M Tasneem, Saba Khan, Shahid Y Griffith, Andrew J Friedman, Thomas B Riazuddin, Sheikh Producer: 20100203 In: Journal of human genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse. [electronic resource] by Yousaf, Rizwan Gu, Chunfang Ahmed, Zubair M Khan, Shaheen N Friedman, Thomas B Riazuddin, Sheikh Shears, Stephen B Riazuddin, Saima Producer: 20180626 In: PLoS genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families. [electronic resource] by Riazuddin, S Amer Yasmeen, Afshan Yao, Wenliang Sergeev, Yuri V Zhang, Qingjiong Zulfiqar, Fareeha Riaz, Assad Riazuddin, Sheikh Hejtmancik, J Fielding Producer: 20050721 In: Investigative ophthalmology & visual science vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene. [electronic resource] by Zhang, Qingjiong Zulfiqar, Fareeha Xiao, Xueshan Riazuddin, S Amer Ahmad, Zahoor Caruso, Raphael MacDonald, Ian Sieving, Paul Riazuddin, Sheikh Hejtmancik, J Fielding Producer: 20080402 In: Human genetics vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Localization of autosomal recessive congenital cataracts in consanguineous Pakistani families to a new locus on chromosome 1p. [electronic resource] by Butt, Tariq Yao, Wenliang Kaul, Haiba Xiaodong, Jiao Gradstein, Libe Zhang, Yan Husnain, Tayyab Riazuddin, Sheikh Hejtmancik, J Fielding Riazuddin, S Amer Producer: 20071023 In: Molecular vision vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	66.	A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12. [electronic resource] by Shaikh, Rehan Sadiq Ramzan, Khushnooda Nazli, Sabiha Sattar, Sameera Khan, Shaheen N Riazuddin, Saima Ahmed, Zubair M Friedman, Thomas B Riazuddin, Sheikh Producer: 20060328 In: American journal of medical genetics. Part A vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Identification of micro-RNAs in cotton. [electronic resource] by Khan Barozai, Muhammad Younas Irfan, Muhammad Yousaf, Rizwan Ali, Imran Qaisar, Uzma Maqbool, Asma Zahoor, Muzna Rashid, Bushra Hussnain, Tayyab Riazuddin, Sheikh Producer: 20081006 In: Plant physiology and biochemistry : PPB vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1. [electronic resource] by Ramzan, Khushnooda Shaikh, Rehan S Ahmad, Jamil Khan, Shaheen N Riazuddin, Saima Ahmed, Zubair M Friedman, Thomas B Wilcox, Edward R Riazuddin, Sheikh Producer: 20050421 In: Human genetics vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1. [electronic resource] by Ahmad, Jamil Khan, Shaheen N Khan, Shahid Y Ramzan, Khushnooda Riazuddin, Saima Ahmed, Zubair M Wilcox, Edward R Friedman, Thomas B Riazuddin, Sheikh Producer: 20050802 In: Human genetics vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	Nucleotide identity and variability among different Pakistani hepatitis C virus isolates. [electronic resource] by Idrees, Muhammad Butt, Sadia Awan, Zunaira Aftab, Mahwish Khubaib, Bushra Rehman, Irshad-Ur Akram, Madiha Manzoor, Sobia Akbar, Haji Rafiqe, Shazia Riazuddin, Sheikh Producer: 20091103 In: Virology journal vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4. [electronic resource] by Zhang, Qingjiong Zulfiqar, Fareeha Xiao, Xueshan Riazuddin, S Amer Ayyagari, Radha Sabar, Farooq Caruso, Raphael Sieving, Paul A Riazuddin, Sheikh Hejtmancik, J Fielding Producer: 20060321 In: Human genetics vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent. [electronic resource] by Rauf, Bushra Irum, Bushra Kabir, Firoz Firasat, Sabika Naeem, Muhammad Asif Khan, Shaheen N Husnain, Tayyab Riazuddin, Sheikh Akram, Javed Riazuddin, S Amer Producer: 20160810 In: Human genome variation vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome. [electronic resource] by Ahmed, Zubair M Riazuddin, Saima Aye, Sandar Ali, Rana A Venselaar, Hanka Anwar, Saima Belyantseva, Polina P Qasim, Muhammad Riazuddin, Sheikh Friedman, Thomas B Producer: 20081024 In: Human genetics vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. [electronic resource] by Hmani-Aifa, Mounira Benzina, Zeineb Zulfiqar, Fareeha Dhouib, Houria Shahzadi, Amber Ghorbel, Abdelmonem Rebaï, Ahmed Söderkvist, Peter Riazuddin, Sheikh Kimberling, William J Ayadi, Hammadi Producer: 20090508 In: European journal of human genetics : EJHG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene. [electronic resource] by Zhang, Qingjiong Zulfiqar, Fareeha Riazuddin, S Amer Xiao, Xueshan Yasmeen, Afshan Rogan, Peter K Caruso, Raphael Sieving, Paul A Riazuddin, Sheikh Hejtmancik, J Fielding Producer: 20060413 In: Molecular vision vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	76.	Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family. [electronic resource] by Shahzadi, Amber Riazuddin, S Amer Ali, Shahbaz Li, David Khan, Shaheen N Husnain, Tayyab Akram, Javed Sieving, Paul A Hejtmancik, J Fielding Riazuddin, Sheikh Producer: 20100819 In: The British journal of ophthalmology vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Hepatitis C virus genotype 3a infection and hepatocellular carcinoma: Pakistan experience. [electronic resource] by Idrees, Muhammad Rafique, Shazia Rehman, Irshadur Akbar, Haji Yousaf, Muhammad-Zubair Butt, Sadia Awan, Zunaira Manzoor, Sobia Akram, Madiha Aftab, Mahwish Khubaib, Bushra Riazuddin, Sheikh Producer: 20100112 In: World journal of gastroenterology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa. [electronic resource] by Ali, Shahbaz Riazuddin, S Amer Shahzadi, Amber Nasir, Idrees A Khan, Shaheen N Husnain, Tayyab Akram, Javed Sieving, Paul A Hejtmancik, J Fielding Riazuddin, Sheikh Producer: 20110926 In: Molecular vision vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	79.	Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy. [electronic resource] by Kabir, Firoz Naz, Shagufta Riazuddin, S Amer Naeem, Muhammad Asif Khan, Shaheen N Husnain, Tayyab Akram, Javed Sieving, Paul A Hejtmancik, J Fielding Riazuddin, Sheikh Producer: 20130924 In: Molecular vision vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	80.	Phenotypic variability associated with the D226N allele of IMPDH1. [electronic resource] by Ali, Shahbaz Khan, Shahid Y Naeem, Muhammad Asif Khan, Shaheen N Husnain, Tayyab Riazuddin, Saima Ayyagari, Radha Riazuddin, Sheikh Hejtmancik, J Fielding Riazuddin, S Amer Producer: 20150414 In: Ophthalmology vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 164 results.