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email:
Faravareh.KhordadpourDeilamani@glasgow.ac.uk
pronouns:
She/her/hers
Khordadpour Deilamani, F. and Taghi Akbari, M. (2022) First report of preimplantation genetic diagnosis of mucopolysaccharidoses IVA and HLA typing for hematopoietic stem cell transplantation. Bulletin of the National Research Centre, 46, 283. (doi: 10.1186/s42269-022-00972-0)
Khordadpour Deilamani, F. and Taghi Akbari, M. (2020) Preimplantation genetic diagnosis for beta thalassemia. Journal of Human Genetics and Genomics, 3(1), e109503. (doi: 10.5812/jhgg.109503)
Khordadpoor Deilamani, F. and Taghi Akbari, M. (2020) First report of preimplantation genetic diagnosis for steroid-resistant nephrotic syndrome. Journal of Human Genetics and Genomics, 3(1), e109109. (doi: 10.5812/jhgg.109109)
Salimy, Z., Akbari, M.T. and Khordadpoor Deilamani, F. (2020) Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency. Journal of Genetics, 99, 6. (doi: 10.1007/s12041-019-1171-5) (PMID:32089525)
Khordadpoor Deilamani, F. and Akbari, M.T. (2016) Population data of 13 nonCODIS STR markers located inside the 6 nonsyndromic oculocutaneous albinism genes. International Journal of Legal Medicine, 130(6), pp. 1485-1486. (doi: 10.1007/s00414-016-1342-3) (PMID:26932870)
Khordadpoor-Deilamani, F. , Akbari, M.T., Karimipoor, M. and Javadi, G.R. (2016) Homozygosity mapping in albinism patients using a novel panel of 13 STR markers inside the nonsyndromic OCA genes: Introducing 5 novel mutations. Journal of Human Genetics, 61(5), pp. 373-379. (doi: 10.1038/jhg.2015.167) (PMID:26818737)
Khordadpour Deilamani, F. and Taghi Akbari, M. (2022) First report of preimplantation genetic diagnosis of mucopolysaccharidoses IVA and HLA typing for hematopoietic stem cell transplantation. Bulletin of the National Research Centre, 46, 283. (doi: 10.1186/s42269-022-00972-0)
Khordadpour Deilamani, F. and Taghi Akbari, M. (2020) Preimplantation genetic diagnosis for beta thalassemia. Journal of Human Genetics and Genomics, 3(1), e109503. (doi: 10.5812/jhgg.109503)
Khordadpoor Deilamani, F. and Taghi Akbari, M. (2020) First report of preimplantation genetic diagnosis for steroid-resistant nephrotic syndrome. Journal of Human Genetics and Genomics, 3(1), e109109. (doi: 10.5812/jhgg.109109)
Salimy, Z., Akbari, M.T. and Khordadpoor Deilamani, F. (2020) Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency. Journal of Genetics, 99, 6. (doi: 10.1007/s12041-019-1171-5) (PMID:32089525)
Khordadpoor Deilamani, F. and Akbari, M.T. (2016) Population data of 13 nonCODIS STR markers located inside the 6 nonsyndromic oculocutaneous albinism genes. International Journal of Legal Medicine, 130(6), pp. 1485-1486. (doi: 10.1007/s00414-016-1342-3) (PMID:26932870)
Khordadpoor-Deilamani, F. , Akbari, M.T., Karimipoor, M. and Javadi, G.R. (2016) Homozygosity mapping in albinism patients using a novel panel of 13 STR markers inside the nonsyndromic OCA genes: Introducing 5 novel mutations. Journal of Human Genetics, 61(5), pp. 373-379. (doi: 10.1038/jhg.2015.167) (PMID:26818737)
https://orcid.org/0000-0002-1779-6135