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Investigative Ophthalmology & Visual Science|August 1, 2006
Screening of the eight BBS genes in Tunisian families: no evidence of triallelismNizar Smaoui, Myriam Chaabouni, Yuri V Sergeev, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|October 12, 2011
Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani familiesMuhammad Iqbal, Muhammad Asif Naeem, S Amer Riazuddin, et al.The Journal of the American Osteopathic Association|December 29, 2006
Multiple aortocoronary bypass saphenous vein graft aneurysms in a 77-year-old manAnne-Marie Moukala-Cadet, Stephen J Mitrosky, Glenn D Miller, et al.Nature Communications|November 30, 2016
Direct visualization of a Fe(IV)-OH intermediate in a heme enzymeHanna Kwon, Jaswir Basran, Cecilia M Casadei, et al.Molecular Vision|January 5, 2011
Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8pNamerah Sabir, S Amer Riazuddin, Haiba Kaul, et al.Molecular Vision|June 17, 2016
Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial casesFiroz Kabir, Inayat Ullah, Shahbaz Ali, et al.The British Journal of Ophthalmology|March 31, 2011
Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani familiesShagufta Naz, Shahbaz Ali, S Amer Riazuddin, et al.Molecular Vision|July 22, 2016
Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial casesInayat Ullah, Firoz Kabir, Muhammad Iqbal, et al.Scientific Data|October 14, 2020
Whole genome sequencing data of multiple individuals of Pakistani descentShahid Y Khan, Muhammad Ali, Mei-Chong W Lee, et al.Molecular Vision|December 24, 2010
Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3qNamerah Sabir, S Amer Riazuddin, Tariq Butt, et al.Pageof 42