Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian population-Reference-Cited by-同舟云学术

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Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian population

Published:2014-03-15 Issue:6 Volume:92 Page:514-520
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Mayuranathan Thiyagaraj¹,Rayabaram Janakiram¹,Das Reena²,Arora Neeraj¹,Edison Eunice S.¹,Chandy Mammen³,Srivastava Alok¹⁴,Velayudhan Shaji R.¹⁴

Affiliation:

1. Department of Haematology; Christian Medical College; Vellore India

2. Postgraduate Institute of Medical Education and Research; Chandigarh India

3. Tata Medical Centre; Kolkata India

4. Centre for Stem Cell Research; Christian Medical College; Vellore India

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.12276/fullpdf

Reference25 articles.

1. The Molecular Basis of β Thalassemia, δβ Thalassemia, and Hereditary Persistence of Fetal Hemoglobin

2. Fetal hemoglobin levels in adults;Rochette;Blood Rev,1994

3. HbVar database of human hemoglobin variants and Thalassemia mutations: 2007 update;Giardine;Hum Mutat,2007

4. Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements;Phylipsen;Hum Mutat,2012

5. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α and β-thalassemia characterized by high-resolution multiplex ligation-dependent probe amplification;Harteveld;J Med Genet,2005

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3. Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin;Pediatric Hematology Oncology Journal;2023-03

4. A Novel Tool for the Analysis and Detection of Copy Number Variants Associated with Haemoglobinopathies;International Journal of Molecular Sciences;2022-12-14

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