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	1.	CLRN1 mutations cause nonsyndromic retinitis pigmentosa. [electronic resource] by Khan, Muhammad Imran Kersten, Ferry F J Azam, Maleeha Collin, Rob W J Hussain, Alamdar Shah, Syed Tahir-A Keunen, Jan E E Kremer, Hannie Cremers, Frans P M Qamar, Raheel den Hollander, Anneke I Producer: 20110905 In: Ophthalmology vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families. [electronic resource] by Shafique, Sobia Siddiqi, Saima Schraders, Margit Oostrik, Jaap Ayub, Humaira Bilal, Ammad Ajmal, Muhammad Seco, Celia Zazo Strom, Tim M Mansoor, Atika Mazhar, Kehkashan Shah, Syed Tahir A Hussain, Alamdar Azam, Maleeha Kremer, Hannie Qamar, Raheel Producer: 20150212 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosa. [electronic resource] by Azam, Maleeha Collin, Rob W J Malik, Ayesha Khan, Muhammad I Shah, Syed Tahir A Shah, Aftab A Hussain, Alamdar Sadeque, Ahmed Arimadyo, Kentar Ajmal, Muhammad Azam, Ayesha Qureshi, Nadeem Bokhari, Habib Strom, Tim M Cremers, Frans P M Qamar, Raheel den Hollander, Anneke I Producer: 20111207 In: Archives of ophthalmology (Chicago, Ill. : 1960) vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)