An interplay of alleviating mutations in the clinical phenotype of beta-thalassaemia intermedia-Reference-Cited by-同舟云学术

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An interplay of alleviating mutations in the clinical phenotype of beta-thalassaemia intermedia

Published:2004-12 Issue:6 Volume:26 Page:419-422
ISSN:0141-9854
Container-title:Clinical and Laboratory Haematology
language:en
Short-container-title:Clin Lab Haematol

Author:

NADKARNI A.,SAKAGUCHI T.,GORAKSHAKAR A.,PHANASGAONKAR S.,KIYAMA R.,COLAH R.,MOHANTY D.

Publisher

Wiley

Subject

Hematology,Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2257.2004.00638.x/fullpdf

Reference13 articles.

1. Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States

2. Potential of denaturing gradient gel electrophoresis for scanning of ?-thalassemia mutations in India

3. A β-thalassaemia phenotype not linked to the β-globin cluster in an Italian family

Cited by 3 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. Cross-Sectional Study for the Detection of Mutations in the Beta-Globin Gene Among Patients with Hemoglobinopathies in the Bengali Population;Genetic Testing and Molecular Biomarkers;2017-01

2. Identification of Two Rare β-Globin Gene Mutations in a Patient with β-Thalassemia Intermedia from Azerbaijan;Hemoglobin;2013-03-19

3. Molecular variants and clinical importance of β-thalassaemia traits found in the state of Orissa, India;Hematology;2009-10

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