β-Thalassemia in iran: A high incidence of the nonsense codon 39 mutation on the island of queshm-Reference-Cited by-同舟云学术

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β-Thalassemia in iran: A high incidence of the nonsense codon 39 mutation on the island of queshm

Published:1994-01 Issue:6 Volume:18 Page:449-453
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Noori-Daloii M. R.,Moazami N.,Farhangi S.,Atalay A.,Geren I. N.,Akar L.,Atalay E. O.,Clirakoglu B.,Bermek E.

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269409045779

Reference18 articles.

1. Delineation of specific beta-thalassemia mutations in high-risk areas of Italy: a prerequisite for prenatal diagnosis

2. Oligonucleotide Screening of β Thalassemia Mutations in the South East of France

3. The peculiar spectrum of ?-thalassemia genes in Tunisia

4. Molecular characterization of β-thalassaemia in 174 Greek patients with thalassaemia major

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1. Sistani Population: a Different Spectrum oF β-Thalassemia Mutations From other Ethnic Groups of Iran;Hemoglobin;2013-02-26

2. Profile of β-Thalassemia and its Prenatal Diagnosis in Khorasan-E-Jonobi Province, Iran;Hemoglobin;2012-06

3. Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration;The Scientific World Journal;2012

4. Molecular basis and prenatal diagnosis of β-thalassemia among Balouch population in Iran;Prenatal Diagnosis;2011-06-21

5. A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population;Blood Cells, Molecules, and Diseases;2011-06

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