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Shakeel A Sheikh

Showing results (1-10 of 5) with videos related to

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IEEE Journal of Biomedical and Health Informatics|April 7, 2023
Advancing Stuttering Detection via Data Augmentation, Class-Balanced Loss and Multi-Contextual Deep LearningShakeel A Sheikh, Md Sahidullah, Fabrice Hirsch, et al.
Genes|April 23, 2022
Delineating the Molecular and Phenotypic Spectrum of the <i>CNGA3</i>-Related Cone Photoreceptor Disorder in Pakistani FamiliesSairah Yousaf, Nabeela Tariq, Zureesha Sajid, et al.
Pigment Cell & Melanoma Research|November 18, 2015
Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani populationSairah Yousaf, Mohsin Shahzad, Tasleem Kausar, et al.
Molecular Vision|March 2, 2019
Identities and frequencies of variants in <i>CYP1B1</i> causing primary congenital glaucoma in PakistanMuhammad Rashid, Sairah Yousaf, Shakeel A Sheikh, et al.
Investigative Ophthalmology & Visual Science|November 20, 2019
Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod DystrophyShakeel A Sheikh, Robert A Sisk, Cara R Schiavon, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
IEEE Journal of Biomedical and Health Informatics|April 7, 2023
Advancing Stuttering Detection via Data Augmentation, Class-Balanced Loss and Multi-Contextual Deep LearningShakeel A Sheikh, Md Sahidullah, Fabrice Hirsch, et al.
Genes|April 23, 2022
Delineating the Molecular and Phenotypic Spectrum of the <i>CNGA3</i>-Related Cone Photoreceptor Disorder in Pakistani FamiliesSairah Yousaf, Nabeela Tariq, Zureesha Sajid, et al.
Pigment Cell & Melanoma Research|November 18, 2015
Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani populationSairah Yousaf, Mohsin Shahzad, Tasleem Kausar, et al.
Molecular Vision|March 2, 2019
Identities and frequencies of variants in <i>CYP1B1</i> causing primary congenital glaucoma in PakistanMuhammad Rashid, Sairah Yousaf, Shakeel A Sheikh, et al.
Investigative Ophthalmology & Visual Science|November 20, 2019
Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod DystrophyShakeel A Sheikh, Robert A Sisk, Cara R Schiavon, et al.
Pageof 1