Search Results - "Mohammadi-Asl, J." :: K.UTB vyhledávací portál

Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome

by Mohammadi‐asl, J., Hajjari, M., Tahmasebi Birgani, M., Riahi, K., Nasiri, H., Kollaee, A.
Published in Annals of human genetics (01.09.2018)

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Quantitative evaluation of DNMT3B promoter methylation in breast cancer patients using differential high resolution melting analysis

by Naghitorabi, M, Mohammadi Asl, J, Mir Mohammad Sadeghi, H, Rabbani, M, Jafarian-Dehkordi, A, Javanmard, Haghjooye S
Published in Research in pharmaceutical sciences (01.07.2013)

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GM2 Gangliosidosis: Whole-Exome Sequencing Reveals Novel Homozygous Pathogenic Variant within the HEXA Gene in Iranian Family

by Zargar, Z., Maleknia, M., Sabzeghabaiean, M., Mohammadi-Asl, J., Golab, F., Naseroleslami, M.
Published in Russian journal of genetics (2024)

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Prevalence of BRAF super(V600E) Mutation in Iranian Patients with Papillary Thyroid Carcinoma: A Single-Center Study

by Mohammadi-Asl, J, Larijani, B, Khorgami, Z, Tavangar, S M, Haghpanah, V, Mehdipour, P
Published in Journal of applied sciences (Asian Network for Scientific Information) (01.01.2009)

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Journal Article

Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome

Quantitative evaluation of DNMT3B promoter methylation in breast cancer patients using differential high resolution melting analysis

GM2 Gangliosidosis: Whole-Exome Sequencing Reveals Novel Homozygous Pathogenic Variant within the HEXA Gene in Iranian Family

Prevalence of BRAF super(V600E) Mutation in Iranian Patients with Papillary Thyroid Carcinoma: A Single-Center Study

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