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Molecular Biology Reports|February 18, 2025
Comprehensive review and outline of genotypes and phenotypes of Arboleda-Tham syndrome spectrum: insights from novel variantsSahar Bayat, Milad Gholami, Hamidreza Khodadadi, et al.European Journal of Medical Genetics|June 20, 2023
ALDH1A3-related congenital microphthalmia-8 due to a novel frameshift variantFahimeh Piryaei, Rezvan Pakmanesh, Maryam Salehirad, et al.Basic and Clinical Neuroscience|July 1, 2026
Expanding the Phenotype and Genotype Spectrum of a Novel Mutation in Hypomyelinating Leukodystrophy-5 With a Review of the Literature on 42 CasesSahar Bayat, Milad Gholami, Hamidreza Khodadadi, et al.Microbial Pathogenesis|May 21, 2022
SARS-COV-2 RBD (Receptor binding domain) mutations and variants (A sectional-analytical study)Faezeh Hajizadeh, Sayyad Khanizadeh, Hamidreza Khodadadi, et al.Iranian Journal of Medical Sciences|February 2, 2026
A Novel AP4M1 Variant in an Iranian Child with Spastic Paraplegia 50: A Case Report and Molecular Docking ApproachHamed Esmaeil Lashgarian, Masumeh Jalalvand, Maryam Zand, et al.Clinical Laboratory|February 18, 2016
A Single Nucleotide Polymorphism in the FOXP3 Gene Associated with Behçet's Disease in an Iranian PopulationArezoo Hosseini, Dariush Shanehbandi, Mehrdad Asghari Estiar, et al.Cold Spring Harbor Molecular Case Studies|June 28, 2017
Identification of a novel mutation in the APTX gene associated with ataxia-oculomotor apraxiaJingga Inlora, M Reza Sailani, Hamidreza Khodadadi, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2016
PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonismHamidreza Khodadadi, Luis J Azcona, Vajiheh Aghamollaii, et al.Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Recessive genomic and phenotypic variation in consanguineous families with cerebral palsyPritha Bisarad, Yung-Chun Wang, Peter T Skidmore, et al.Pageof 1