Literature DB >> 12368169

Rare and unexpected mutations among Iranian beta-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing.

Hossein Najmabadi, Ali A Pourfathollah, Maryam Neishabury, Farhad Sahebjam, Walter Krugluger, Christian Oberkanins.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2002        PMID： 12368169

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


× No keyword cloud information.
  4 in total

1.  High prevalence of rare mutations in the Beta globin gene in an ethnic group in iran.

Authors:  H Galehdari; B Salehi; M Pedram; M Oraki Kohshour
Journal:  Iran Red Crescent Med J       Date:  2011-05-01       Impact factor: 0.611

2.  Tetra-Primer ARMS PCR Optimization for Detection of IVS-II-I (G-A) and FSC 8/9 InsG Mutations in β-Thalassemia Major Patients in Isfahan Population.

Authors:  Samaneh Hajihoseini; Majid Motovali-Bashi; Mohammad Amin Honardoost; Nader Alerasool
Journal:  Iran J Public Health       Date:  2015-03       Impact factor: 1.429

3.  Beta-Thalassemia in Iran: new insight into the role of genetic admixture and migration.

Authors:  Ali Reza Rezaee; Mohammad Mehdi Banoei; Elham Khalili; Massoud Houshmand
Journal:  ScientificWorldJournal       Date:  2012-12-18

Review 4.  Hemoglobinopathies in Iran: An Updated Review.

Authors:  Abolfazl Nasiri; Zohreh Rahimi; Asad Vaisi-Raygani
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2020-04-01
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.