Showing 1 - 3 results of 3 for search 'Kehkashan Mazhar', query time: 0.03s
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Molecular diagnosis of Fragile X syndrome in subjects with intellectual disability of unknown origin: implications of its prevalence in regional Pakistan. by Madiha Kanwal, Saadia Alyas, Muhammad Afzal, Atika Mansoor, Rashda Abbasi, Flora Tassone, Sajid Malik, Kehkashan Mazhar
Published 2015-01-01
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Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families. by Sobia Shafique, Saima Siddiqi, Margit Schraders, Jaap Oostrik, Humaira Ayub, Ammad Bilal, Muhammad Ajmal, Celia Zazo Seco, Tim M Strom, Atika Mansoor, Kehkashan Mazhar, Syed Tahir A Shah, Alamdar Hussain, Maleeha Azam, Hannie Kremer, Raheel Qamar
Published 2014-01-01
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