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Ophthalmic Genetics|November 23, 2019
Next-generation sequencing and its application in diagnosis of retinitis pigmentosaArash Salmaninejad, Jamshid Motaee, Mahsa Farjami, et al.
Clinical Biochemistry|August 7, 2017
Paraoxonase 1 (PON1) and stroke; the dilemma of genetic variationAmir Tajbakhsh, Mehdi Rezaee, Mahdi Rivandi, et al.
Viral Immunology|August 15, 2014
Haplotype analysis of interleukin-10 gene promoter polymorphisms in chronic hepatitis C infection: a case control studySamaneh Sepahi, Alireza Pasdar, Mitra Ahadi, et al.
Reports of Biochemistry & Molecular Biology|November 2, 2017
CTLA-4 Gene Haplotypes and the Risk of Chronic Hepatitis C Infection; a Case Control StudySamaneh Sepahi, Alireza Pasdar, Sina Gerayli, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|January 13, 2023
Genetic architecture of mammographic density as a risk factor for breast cancer: a systematic reviewAsma Khorshid Shamshiri, Maryam Alidoust, Mahboubeh Hemmati Nokandei, et al.
Journal of Current Ophthalmology|September 8, 2023
Identification of a Missense Mutation in GJA8 Gene in an Iranian Family with Autosomal Dominant Congenital CataractMahla Asghari, Soheila Abedini, Melika Farshidianfar, et al.
IUBMB Life|November 15, 2019
A novel mutation in USF1 gene is associated with familial combined hyperlipidemiaEskandar Taghizadeh, Farzaneh Mirzaei, Nazanin Jalilian, et al.
Annals of Medicine|August 1, 2020
Personalised medicine in hypercholesterolaemia: the role of pharmacogenetics in statin therapyNajmeh Ahangari, Mohammad Doosti, Majid Ghayour Mobarhan, et al.
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