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Sadaf Naz

Showing results (1-10 of 89) with videos related to

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Human Genetics|July 26, 2021
Molecular genetic landscape of hereditary hearing loss in PakistanSadaf Naz
Parkinsonism & Related Disorders|May 4, 2019
Ataxia and dysarthria due to an ABCA2 variant: Extension of the phenotypic spectrumFaiza Aslam, Sadaf Naz
Neurogenetics|January 27, 2017
TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrumHuma Tariq, Sadaf Naz
Pakistan Journal of Zoology|October 21, 2014
A Rapid and Cost-Effective Protocol for Screening Known Genes for Autosomal Recessive DeafnessAyesha Imtiaz, Sadaf Naz
Molecular Biotechnology|May 31, 2012
Amplification of GC-rich DNA for high-throughput family-based genetic studiesSadaf Naz, Amara Fatima
Clinical Genetics|September 12, 2019
Growth factor and receptor malfunctions associated with human genetic deafnessSadaf Naz, Thomas B Friedman
Biochemical Genetics|March 19, 2013
Contribution of GJB2 mutations to hearing loss in the Hazara Division of PakistanIhtisham Bukhari, Ghulam Mujtaba, Sadaf Naz
Journal of Neurogenetics|May 16, 2017
A novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysisHuma Tariq, Shahid Mukhtar, Sadaf Naz
Journal 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 Naz
BMC Musculoskeletal Disorders|January 7, 2021
Spondylocarpotarsal synostosis syndrome due to a novel loss of function FLNB variant: a case reportSamina Yasin, Outi Makitie, Sadaf Naz
Pageof 9

Showing results (1-10 of 89) with videos related to

Sort By:
Pageof 9
Human Genetics|July 26, 2021
Molecular genetic landscape of hereditary hearing loss in PakistanSadaf Naz
Parkinsonism & Related Disorders|May 4, 2019
Ataxia and dysarthria due to an ABCA2 variant: Extension of the phenotypic spectrumFaiza Aslam, Sadaf Naz
Neurogenetics|January 27, 2017
TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrumHuma Tariq, Sadaf Naz
Pakistan Journal of Zoology|October 21, 2014
A Rapid and Cost-Effective Protocol for Screening Known Genes for Autosomal Recessive DeafnessAyesha Imtiaz, Sadaf Naz
Molecular Biotechnology|May 31, 2012
Amplification of GC-rich DNA for high-throughput family-based genetic studiesSadaf Naz, Amara Fatima
Clinical Genetics|September 12, 2019
Growth factor and receptor malfunctions associated with human genetic deafnessSadaf Naz, Thomas B Friedman
Biochemical Genetics|March 19, 2013
Contribution of GJB2 mutations to hearing loss in the Hazara Division of PakistanIhtisham Bukhari, Ghulam Mujtaba, Sadaf Naz
Journal of Neurogenetics|May 16, 2017
A novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysisHuma Tariq, Shahid Mukhtar, Sadaf Naz
Journal 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 Naz
BMC Musculoskeletal Disorders|January 7, 2021
Spondylocarpotarsal synostosis syndrome due to a novel loss of function FLNB variant: a case reportSamina Yasin, Outi Makitie, Sadaf Naz
Pageof 9