Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia-Reference-Cited by-同舟云学术

Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia

Published:1992-01 Issue:1-2 Volume:16 Page:51-66
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

George E.,Li H-J.,Fei Y-J.,Reese A. L.,Baysal E.,Cepreganova B.,Wilson J. B.,Gu L-H.,Nechtman J. F.,Stoming T. A.,Liu J-C.,Codrington J. F.,Huisman T. H. J.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269209005676

Reference36 articles.

1. Molecular characterization of β-globin gene mutations in Malay patients with Hb E-β-thalassaemia and thalassaemia major

2. Two novel polyadenylation mutations leading to β+-thalassaemia

3. A molecular marker associated with mild hemoglobin H disease

Cited by 33 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. HBB Gene Mutations and Their Pathological Impacts on HbE/β-Thalassaemia in Kuala Terengganu, Malaysia;Diagnostics;2023-03-26

2. β-Hemoglobinopathies and Early Onset of Cancers in Adulthood: Epidemiology in Southeastern Asia and Brunei with Emphasis for Prevention and Treatment;Hereditary Gastric and Breast Cancer Syndrome;2023

3. Direct sequencing of β-globin gene reveals a rare combination of two exonic and two intronic variants in a β-thalassemia major patient: a case report;Journal of Medical Case Reports;2022-10-09

4. Characterization of β-Globin Gene Cluster Deletions Using Multiplex-Gap Polymerase Chain Reaction (PCR) and Multiplex Ligation-Dependent Probe Amplification (MLPA);Bangladesh Journal of Medical Science;2021-04-04

5. A Novel Frameshift Mutation, Deletion of HBB:c.199_202delAAAG [Codon 66/67 (-AAAG)] in β-Thalassemia Major Patients from the Western Region of Uttar Pradesh, India;The Application of Clinical Genetics;2021-03