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Sadaf Naz

Showing results (11-20 of 89) with videos related to

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Journal of Human Genetics|September 3, 2010
Mutations in CLDN14 are associated with different hearing thresholdsRasheeda Bashir, Amara Fatima, Sadaf Naz
European 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 Naz
Biochemical Genetics|March 19, 2013
SLC26A4 mutations in patients with moderate to severe hearing lossMuhammad Riaz Khan, Rasheeda Bashir, Sadaf Naz
Journal of Psychiatry & Neuroscience : JPN|November 1, 2022
<i>RGS3</i> and <i>IL1RAPL1</i> missense variants implicate defective neurotransmission in early-onset inherited schizophreniasAmbreen Kanwal, José V Pardo, Sadaf Naz
Biology|April 13, 2026
Genetic Variants from Large Cohorts and Familial Studies Implicate Common Mechanisms in SchizophreniaAmbreen Kanwal, José V Pardo, Sadaf Naz
Human Mutation|March 13, 2014
A frameshift mutation in GRXCR2 causes recessively inherited hearing lossAyesha Imtiaz, David C Kohrman, Sadaf Naz
Journal of Medical Genetics|August 24, 2017
Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic <i>COL10A1</i> variantNoor Ul Ain, Outi Makitie, Sadaf Naz
European Journal of Medical Genetics|September 16, 2019
RIN2 and BBS7 variants as cause of a coincidental syndromeMemoona Shaukat, Tayyaba Ishaq, Niaz Muhammad, et al.
Gene|May 24, 2012
A p.C343S missense mutation in PJVK causes progressive hearing lossGhulam Mujtaba, Ihtisham Bukhari, Amara Fatima, et al.
International Journal of Biological Macromolecules|December 3, 2023
Applications of guar gum polysaccharide for pharmaceutical drug delivery: A reviewNyla Amjed, Muhammad Zeshan, Ariba Farooq, et al.
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
Journal of Human Genetics|September 3, 2010
Mutations in CLDN14 are associated with different hearing thresholdsRasheeda Bashir, Amara Fatima, Sadaf Naz
European 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 Naz
Biochemical Genetics|March 19, 2013
SLC26A4 mutations in patients with moderate to severe hearing lossMuhammad Riaz Khan, Rasheeda Bashir, Sadaf Naz
Journal of Psychiatry & Neuroscience : JPN|November 1, 2022
<i>RGS3</i> and <i>IL1RAPL1</i> missense variants implicate defective neurotransmission in early-onset inherited schizophreniasAmbreen Kanwal, José V Pardo, Sadaf Naz
Biology|April 13, 2026
Genetic Variants from Large Cohorts and Familial Studies Implicate Common Mechanisms in SchizophreniaAmbreen Kanwal, José V Pardo, Sadaf Naz
Human Mutation|March 13, 2014
A frameshift mutation in GRXCR2 causes recessively inherited hearing lossAyesha Imtiaz, David C Kohrman, Sadaf Naz
Journal of Medical Genetics|August 24, 2017
Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic <i>COL10A1</i> variantNoor Ul Ain, Outi Makitie, Sadaf Naz
European Journal of Medical Genetics|September 16, 2019
RIN2 and BBS7 variants as cause of a coincidental syndromeMemoona Shaukat, Tayyaba Ishaq, Niaz Muhammad, et al.
Gene|May 24, 2012
A p.C343S missense mutation in PJVK causes progressive hearing lossGhulam Mujtaba, Ihtisham Bukhari, Amara Fatima, et al.
International Journal of Biological Macromolecules|December 3, 2023
Applications of guar gum polysaccharide for pharmaceutical drug delivery: A reviewNyla Amjed, Muhammad Zeshan, Ariba Farooq, et al.
Pageof 9