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Pakistan Journal of Zoology|October 21, 2014
A Rapid and Cost-Effective Protocol for Screening Known Genes for Autosomal Recessive DeafnessAyesha Imtiaz, Sadaf NazHuman Mutation|March 13, 2014
A frameshift mutation in GRXCR2 causes recessively inherited hearing lossAyesha Imtiaz, David C Kohrman, Sadaf NazBiochemical Genetics|January 24, 2013
The c.42_52del11 mutation in TPRN and progressive hearing loss in a family from PakistanRasheeda Bashir, Ayesha Imtiaz, Amara Fatima, et al.European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|February 1, 2015
Mutations of GJB2 encoding connexin 26 contribute to non-syndromic moderate and severe hearing loss in PakistanMidhat Salman, Rasheeda Bashir, Ayesha Imtiaz, et al.Journal of Medical Genetics|May 6, 2015
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing lossGhulam Mujtaba, Julie M Schultz, Ayesha Imtiaz, et al.Neurogenetics|February 17, 2016
Recessive mutations of TMC1 associated with moderate to severe hearing lossAyesha Imtiaz, Azra Maqsood, Atteeq U Rehman, et al.Human Genetics|July 26, 2021
Molecular genetic landscape of hereditary hearing loss in PakistanSadaf NazMolecular Genetics and Genomics : MGG|July 23, 2022
ARNSHL gene identification: past, present and futureAyesha ImtiazParkinsonism & Related Disorders|May 4, 2019
Ataxia and dysarthria due to an ABCA2 variant: Extension of the phenotypic spectrumFaiza Aslam, Sadaf NazNeurogenetics|January 27, 2017
TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrumHuma Tariq, Sadaf NazPageof 12