Faravareh Khordadpoor Deilamani

Study of the p.V617F and Exon 12 Mutations in JAK2 Gene Among Iranian Chronic Myeloproliferative Patients

Shohreh Zare Karizi, M. Akbari, S. Z. Karizi, 2019 .

First Report of Preimplantation Genetic Diagnosis for Steroid-Resistant Nephrotic Syndrome

M. Akbari, Faravareh Khordadpoor Deilamani, 2020, Journal of Human Genetics and Genomics.

Assessment of FMR1 triplet repeats in patients affected with mental retardation, fragile X syndrome and primary ovarian insufficiency

M. Akbari, Faravareh Khordadpoor Deilamani, Zeinab Salimy, 2020, Journal of Genetics.

First report of preimplantation genetic diagnosis of mucopolysaccharidoses IVA and HLA typing for hematopoietic stem cell transplantation

M. Akbari, Faravareh Khordadpoor Deilamani, 2022, Bulletin of the National Research Centre.

Preimplantation Genetic Diagnosis for Beta Thalassemia

M. Akbari, Faravareh Khordadpoor Deilamani, 2020, Journal of Human Genetics and Genomics.