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Molecular Biology Reports|June 1, 2024
Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritanceBehnoosh Tasharrofi, Ali Najafi, Elham Pourbakhtyaran, et al.International Journal of Pediatric Otorhinolaryngology|November 22, 2011
Cochlear implant outcomes in children with motor developmental delaySusan Amirsalari, Jaleh Yousefi, Shokofeh Radfar, et al.Archives of Iranian Medicine|July 1, 2014
Investigation of microdeletions in syndromic intellectual disability by MLPA in Iranian populationHoura Loghmani Khouzani, Ariana Kariminejad, Gholamreza Zamani, et al.Fetal and Pediatric Pathology|April 4, 2019
Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen SyndromeSamaneh Vojdani, Susan Amirsalari, Saman Milanizadeh, et al.Iranian Journal of Child Neurology|March 26, 2014
Clinical and Para clinical Manifestations of Tuberous Sclerosis: A Cross Sectional Study on 81 Pediatric PatientsSeyyed Hassan Tonekaboni, Seyyed Hassan Tonekaboni, Parviz Tousi, et al.Journal of Neuromuscular Diseases|February 13, 2023
The First Report of Iranian Registry of Patients with Spinal Muscular AtrophyVahid Mansouri, Morteza Heidari, Maryam Bemanalizadeh, et al.Pageof 4