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Molecular Biotechnology|May 31, 2012
Amplification of GC-rich DNA for high-throughput family-based genetic studiesSadaf Naz, Amara FatimaThe Journal of Biological Chemistry|November 27, 2025
A truncated CDC14A retains catalytic structure and phosphatase activity preserving male fertility but causes nonsyndromic deafnessKanwal Shabbir, Gina Jackisch, Inna A Belyantseva, et al.Clinical Genetics|September 12, 2019
Growth factor and receptor malfunctions associated with human genetic deafnessSadaf Naz, Thomas B FriedmanBiochemical Genetics|March 19, 2013
Contribution of GJB2 mutations to hearing loss in the Hazara Division of PakistanIhtisham Bukhari, Ghulam Mujtaba, Sadaf NazJournal of Neurogenetics|May 16, 2017
A novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysisHuma Tariq, Shahid Mukhtar, Sadaf NazJournal of Clinical Neurology (Seoul, Korea)|September 11, 2018
A Novel Homozygous Variant of SETX Causes Ataxia with Oculomotor Apraxia Type 2Huma Tariq, Rashid Imran, Sadaf NazBMC Musculoskeletal Disorders|January 7, 2021
Spondylocarpotarsal synostosis syndrome due to a novel loss of function FLNB variant: a case reportSamina Yasin, Outi Makitie, Sadaf NazJournal of Human Genetics|September 3, 2010
Mutations in CLDN14 are associated with different hearing thresholdsRasheeda Bashir, Amara Fatima, Sadaf NazEuropean Journal of Medical Genetics|January 17, 2012
Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing lossRasheeda Bashir, Amara Fatima, Sadaf NazBiochemical Genetics|March 19, 2013
SLC26A4 mutations in patients with moderate to severe hearing lossMuhammad Riaz Khan, Rasheeda Bashir, Sadaf NazPageof 12