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Seyedeh Sedigheh Abedini

Showing results (1-10 of 33) with videos related to

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Avicenna Journal of Medical Biotechnology|October 5, 2020
Screening <i>PAX9</i>, <i>MSX1</i> and <i>WNT10A</i> Mutations in 4 Iranian Families with Non-Syndromic Tooth AgenesisShiva Safari, Asghar Ebadifar, Hossien Najmabadi, et al.
Archives of Iranian Medicine|November 13, 2018
tRNA Methyltransferase Defects and Intellectual DisabilitySeyedeh Sedigheh Abedini, Kimia Kahrizi, Lluis Ribas de Pouplana, et al.
Blood Cells, Molecules & Diseases|January 15, 2011
Analyzing 5'HS3 and 5'HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutationsMaryam Neishabury, Azita Azarkeivan, Christian Oberkanins, et al.
Journal of Dental Research, Dental Clinics, Dental Prospects|December 23, 2022
Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontiaShiva Safari, Asghar Ebadifar, Hossien Najmabadi, et al.
Archives of Iranian Medicine|October 8, 2015
Carrier Testing in Known Autosomal Recessive Intellectual Disability Genes in an Iranian Healthy Individual Using Exome SequencingZohreh Mehrjoo, Mohammad Reza Akbari, Seyedeh Sedigheh Abedini, et al.
Hemoglobin|August 7, 2023
The Spectrum of <i>HBB</i> Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-IranNiloofar Bazazzadegan, Seyedeh Sedigheh Abedini, Azita Azarkeivan, et al.
Blood Cells, Molecules & Diseases|November 1, 2011
The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5'HS4Maryam Neishabury, Shahbaz Zamani, Azita Azarkeivan, et al.
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|May 30, 2015
Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's DiseaseZohreh Mehrjoo, Amin Najmabadi, Seyedeh Sedigheh Abedini, et al.
Archives of Iranian Medicine|January 6, 2015
Report of a patient with limb-girdle muscular dystrophy, ptosis and ophthalmoparesis caused by plectinopathyZohreh Fattahi, Kimia Kahrizi, Shahriar Nafissi, et al.
American Journal of Medical Genetics. Part A|December 15, 2018
GPR126: A novel candidate gene implicated in autosomal recessive intellectual disabilityMasoumeh Hosseini, Zohreh Fattahi, Seyedeh Sedigheh Abedini, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Avicenna Journal of Medical Biotechnology|October 5, 2020
Screening <i>PAX9</i>, <i>MSX1</i> and <i>WNT10A</i> Mutations in 4 Iranian Families with Non-Syndromic Tooth AgenesisShiva Safari, Asghar Ebadifar, Hossien Najmabadi, et al.
Archives of Iranian Medicine|November 13, 2018
tRNA Methyltransferase Defects and Intellectual DisabilitySeyedeh Sedigheh Abedini, Kimia Kahrizi, Lluis Ribas de Pouplana, et al.
Blood Cells, Molecules & Diseases|January 15, 2011
Analyzing 5'HS3 and 5'HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutationsMaryam Neishabury, Azita Azarkeivan, Christian Oberkanins, et al.
Journal of Dental Research, Dental Clinics, Dental Prospects|December 23, 2022
Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontiaShiva Safari, Asghar Ebadifar, Hossien Najmabadi, et al.
Archives of Iranian Medicine|October 8, 2015
Carrier Testing in Known Autosomal Recessive Intellectual Disability Genes in an Iranian Healthy Individual Using Exome SequencingZohreh Mehrjoo, Mohammad Reza Akbari, Seyedeh Sedigheh Abedini, et al.
Hemoglobin|August 7, 2023
The Spectrum of <i>HBB</i> Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-IranNiloofar Bazazzadegan, Seyedeh Sedigheh Abedini, Azita Azarkeivan, et al.
Blood Cells, Molecules & Diseases|November 1, 2011
The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5'HS4Maryam Neishabury, Shahbaz Zamani, Azita Azarkeivan, et al.
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|May 30, 2015
Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's DiseaseZohreh Mehrjoo, Amin Najmabadi, Seyedeh Sedigheh Abedini, et al.
Archives of Iranian Medicine|January 6, 2015
Report of a patient with limb-girdle muscular dystrophy, ptosis and ophthalmoparesis caused by plectinopathyZohreh Fattahi, Kimia Kahrizi, Shahriar Nafissi, et al.
American Journal of Medical Genetics. Part A|December 15, 2018
GPR126: A novel candidate gene implicated in autosomal recessive intellectual disabilityMasoumeh Hosseini, Zohreh Fattahi, Seyedeh Sedigheh Abedini, et al.
Pageof 4