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Saima Riazuddin

Showing results (11-20 of 134) with videos related to

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Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical manifestations of DFNB29 deafnessZubair M Ahmed, Saima Riazuddin, Thomas B Friedman, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Genetic modifiers of hereditary hearing lossSaima Riazuddin, Zubair M Ahmed, Thomas B Friedman, et al.
European Journal of Human Genetics : EJHG|November 9, 2021
Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectual disabilityAmama Ghaffar, Faiza Rasheed, Muhammad Rashid, et al.
Plos One|November 25, 2015
Radioprotective Effect of Aminothiol PrC-210 on Irradiated Inner Ear of Guinea PigArnaud P J Giese, Jess G Guarnaschelli, Jonette A Ward, et al.
Genes|August 27, 2020
Novel Mutations in <i>CLPP</i>, <i>LARS2</i>, <i>CDH23</i>, and <i>COL4A5</i> Identified in Familial Cases of Prelingual Hearing LossSaba Zafar, Mohsin Shahzad, Rafaqat Ishaq, et al.
International Journal of Molecular Sciences|January 11, 2022
Novel Homozygous Missense Variant in <i>GJA3</i> Connexin Domain Causing Congenital Nuclear and Cortical CataractsAbdullah Y Hassan, Sairah Yousaf, Moran R Levin, et al.
International Journal of Molecular Sciences|October 13, 2021
Biallelic Variants in <i>EPHA2</i> Identified in Three Large Inbred Families with Early-Onset CataractPriya Jarwar, Shakeel Ahmed Sheikh, Yar Muhammad Waryah, et al.
International Journal of Molecular Sciences|May 27, 2026
Identification of Pathogenic Variants in <i>CYP4F22</i>, <i>FLG</i>, <i>ALOX12B</i>, and <i>NIPAL4</i> in a Case Series of Inherited IchthyosisMalali Abdul Sattar, Amna Aurang Zaib, Huda Abbasi, et al.
Biomolecules|May 27, 2026
Molecular Characterization of Syndromic Hearing Loss in North African Moroccan FamiliesKhawla El Fizazi, Amama Ghaffar, Laila Bouguenouch, et al.
Plos Genetics|March 29, 2018
Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouseRizwan Yousaf, Chunfang Gu, Zubair M Ahmed, et al.
Pageof 14

Showing results (11-20 of 134) with videos related to

Sort By:
Pageof 14
Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical manifestations of DFNB29 deafnessZubair M Ahmed, Saima Riazuddin, Thomas B Friedman, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Genetic modifiers of hereditary hearing lossSaima Riazuddin, Zubair M Ahmed, Thomas B Friedman, et al.
European Journal of Human Genetics : EJHG|November 9, 2021
Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectual disabilityAmama Ghaffar, Faiza Rasheed, Muhammad Rashid, et al.
Plos One|November 25, 2015
Radioprotective Effect of Aminothiol PrC-210 on Irradiated Inner Ear of Guinea PigArnaud P J Giese, Jess G Guarnaschelli, Jonette A Ward, et al.
Genes|August 27, 2020
Novel Mutations in <i>CLPP</i>, <i>LARS2</i>, <i>CDH23</i>, and <i>COL4A5</i> Identified in Familial Cases of Prelingual Hearing LossSaba Zafar, Mohsin Shahzad, Rafaqat Ishaq, et al.
International Journal of Molecular Sciences|January 11, 2022
Novel Homozygous Missense Variant in <i>GJA3</i> Connexin Domain Causing Congenital Nuclear and Cortical CataractsAbdullah Y Hassan, Sairah Yousaf, Moran R Levin, et al.
International Journal of Molecular Sciences|October 13, 2021
Biallelic Variants in <i>EPHA2</i> Identified in Three Large Inbred Families with Early-Onset CataractPriya Jarwar, Shakeel Ahmed Sheikh, Yar Muhammad Waryah, et al.
International Journal of Molecular Sciences|May 27, 2026
Identification of Pathogenic Variants in <i>CYP4F22</i>, <i>FLG</i>, <i>ALOX12B</i>, and <i>NIPAL4</i> in a Case Series of Inherited IchthyosisMalali Abdul Sattar, Amna Aurang Zaib, Huda Abbasi, et al.
Biomolecules|May 27, 2026
Molecular Characterization of Syndromic Hearing Loss in North African Moroccan FamiliesKhawla El Fizazi, Amama Ghaffar, Laila Bouguenouch, et al.
Plos Genetics|March 29, 2018
Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouseRizwan Yousaf, Chunfang Gu, Zubair M Ahmed, et al.
Pageof 14