Hb ANTALYA [CODONS 3–5 (Leu-Thr-Pro → Ser-Asp-Ser)]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA AND HIGH Hb A2-Reference-Cited by-同舟云学术

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Hb ANTALYA [CODONS 3–5 (Leu-Thr-Pro → Ser-Asp-Ser)]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA AND HIGH Hb A2

Published:2001-01 Issue:4 Volume:25 Page:369-373
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Keser Ibrahim,Kayisli Ozlem G.,Yesilipek Akif,Ozes Osman N.,Luleci Guven

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-100107873

Reference14 articles.

1. The β-Thalassemias

2. Trent R. J. Medical Genetics. Molecular Medicine Longman Singapore, Ltd, Singapore 1997; 37–71

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Abnormal hemoglobins associated with the beta-globin gene in Antalya province, Turkey;Turkish Journal of Medical Sciences;2010-01-01

2. Combination of Hb Knossos [Cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish Patient with Beta-Thalassemia Major;Genetic Testing;2007-09

3. Two rare mutations in Turkey: IVS I.130(G-C) and IVS II.848(C-A);Clinical and Laboratory Haematology;2005-08

4. COMBINATION OF IVS2.849 A-G WITH IVS1.1 G-A: A Mutation of β-Globin Gene in a Turkish β-Thalessemia Major Patient;Pediatric Hematology and Oncology;2005-01

5. Molecular Analysis of Beta-Thalassemia and Sickle Cell Anemia in Antalya;Acta Haematologica;2004

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