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Kimia Kahrizi

Showing results (1-10 of 171) with videos related to

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International Journal of Pediatric Otorhinolaryngology|October 5, 2014
Genetics of non-syndromic hearing loss in the Middle EastHossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|April 26, 2018
Calpains: Diverse Functions but EnigmaticMasoumeh Hosseini, Hossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|May 15, 2016
Genetic Studies in Intellectual Disability and Behavioral ImpairmentHoda Mehregan, Hossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|April 18, 2018
Intellectual Disability and Ataxia: Genetic CollisionsSomayeh Kazeminasab, Hossein Najmabadi, Kimia Kahrizi
Journal of Genetics|October 7, 2015
Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian familiesZohreh Mehrjoo, Mojgan Babanejad, Kimia Kahrizi, et al.
Neuroscience|February 12, 2019
Whole-Transcriptome Analysis Reveals Dysregulation of Actin-Cytoskeleton Pathway in Intellectual Disability PatientsKolsoum InanlooRahatloo, Fatemeh Peymani, Kimia Kahrizi, et al.
Journal of Applied Genetics|January 23, 2025
Genetic etiology of Perrault syndrome in Iranian families: first report from Iran and literature reviewEbrahim Shokouhian, Kimia Kahrizi, Hossein Najmabadi, et al.
Iranian Biomedical Journal|April 9, 2008
The frequency of eight common point mutations in CYP21 gene in Iranian patients with congenital adrenal hyperplasiaAli Ramazani, Kimia Kahrizi, Maryam Razaghiazar, et al.
Clinical Genetics|August 28, 2025
FSCN1 as a Candidate Gene for Syndromic Intellectual Disability? Evidence From a Recurrent Variant in an Iranian CohortHossein Najmabadi, Tara Akhtarkhavari, Ebrahim Shokouhian, et al.
Archives of Iranian Medicine|November 24, 2021
The <i>PTRHD1</i> Mutation in Intellectual DisabilitySara Cheraghi, Sahar Moghbelinejad, Hossein Najmabadi, et al.
Pageof 18

Showing results (1-10 of 171) with videos related to

Sort By:
Pageof 18
International Journal of Pediatric Otorhinolaryngology|October 5, 2014
Genetics of non-syndromic hearing loss in the Middle EastHossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|April 26, 2018
Calpains: Diverse Functions but EnigmaticMasoumeh Hosseini, Hossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|May 15, 2016
Genetic Studies in Intellectual Disability and Behavioral ImpairmentHoda Mehregan, Hossein Najmabadi, Kimia Kahrizi
Archives of Iranian Medicine|April 18, 2018
Intellectual Disability and Ataxia: Genetic CollisionsSomayeh Kazeminasab, Hossein Najmabadi, Kimia Kahrizi
Journal of Genetics|October 7, 2015
Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian familiesZohreh Mehrjoo, Mojgan Babanejad, Kimia Kahrizi, et al.
Neuroscience|February 12, 2019
Whole-Transcriptome Analysis Reveals Dysregulation of Actin-Cytoskeleton Pathway in Intellectual Disability PatientsKolsoum InanlooRahatloo, Fatemeh Peymani, Kimia Kahrizi, et al.
Journal of Applied Genetics|January 23, 2025
Genetic etiology of Perrault syndrome in Iranian families: first report from Iran and literature reviewEbrahim Shokouhian, Kimia Kahrizi, Hossein Najmabadi, et al.
Iranian Biomedical Journal|April 9, 2008
The frequency of eight common point mutations in CYP21 gene in Iranian patients with congenital adrenal hyperplasiaAli Ramazani, Kimia Kahrizi, Maryam Razaghiazar, et al.
Clinical Genetics|August 28, 2025
FSCN1 as a Candidate Gene for Syndromic Intellectual Disability? Evidence From a Recurrent Variant in an Iranian CohortHossein Najmabadi, Tara Akhtarkhavari, Ebrahim Shokouhian, et al.
Archives of Iranian Medicine|November 24, 2021
The <i>PTRHD1</i> Mutation in Intellectual DisabilitySara Cheraghi, Sahar Moghbelinejad, Hossein Najmabadi, et al.
Pageof 18