Alireza Kordafshari

发表

Molecular Basis of α-Thalassemia in Iran

S. Zeinali, M. Karimipoor, A. Valaei, 2018, Iranian biomedical journal.

Molecular Characterization of δ-Thalassemia in Iran

S. Zeinali, M. Karimipoor, A. Amirian, 2016, Hemoglobin.

Co-inheritance of α-and β-thalassemia : challenges in prenatal diagnosis of thalassemia

S. Zeinali, M. Karimipoor, A. Valaei, 2012 .

The Carrier Frequency of α-Globin Gene Triplication in an Iranian Population with Normal or Borderline Hematological Parameters

S. Zeinali, S. Moosavi, M. Karimipoor, 2011, Hemoglobin.

Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevance.

S. Zeinali, Leila Katouzian, M. Karimipoor, 2011, Archives of Iranian medicine.

First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.

S. Zeinali, M. Karimipoor, A. Amirian, 2011, Archives of Iranian medicine.

Identification of a Novel δ-Globin Gene Mutation in an Iranian Family

S. Zeinali, M. Karimipoor, A. Amirian, 2010, Hemoglobin.

A Novel Polymorphism Causes A Different Restriction Pattern by RsaI in the β-Globin Gene Cluster: Application in Prenatal Diagnosis

S. Zeinali, M. Karimipoor, A. Valaei, 2009, Hemoglobin.

Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families

S. Zeinali, S. Saber, A. Fazelifar, 2019, Iranian biomedical journal.

Identifying and predicting the pathogenic effects of a novel variant inducing severe early onset MMA: a bioinformatics approach

H. Rahimi, S. Zeinali, S. Talebi, 2023, Hereditas.

Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population

S. Zeinali, M. Karimipoor, Z. Sharifi, 2019, Turkish journal of medical sciences.