Combine-ARMS: A Rapid and Cost-Effective Protocol for Molecular Characterization of β-Thalassemia in Malaysia-Reference-Cited by-同舟云学术

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Combine-ARMS: A Rapid and Cost-Effective Protocol for Molecular Characterization of β-Thalassemia in Malaysia

Published:2001-03 Issue:1 Volume:5 Page:17-22
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Tan K.L.¹,Tan J.A.M.A.¹,Wong Y.C.¹,Wee Y.C.¹,Thong M.K.²,Yap S.F.³

Affiliation:

1. Department of Allied Health Sciences, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia

2. Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia

3. Department of Pathology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/109065701750168626

Reference12 articles.

1. Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification

2. Multiplex Mutagenically Separated PCR: Diagnosis of β-Thalassemia and Hemoglobin Variants

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

4. Treatment of β-thalassemia

5. Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families

Cited by 14 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. ß-globin Gene Mutations Among ß-thalassemia and ß-variant patients in a teaching Hospital in Universiti Sains Malaysia, Kubang Kerian, Kelantan;Gazi Medical Journal;2022-07-01

2. Towards a Prevention Program for β-Thalassemia. The Molecular Spectrum in East Java, Indonesia;Hemoglobin;2011-12-21

3. Prenatal diagnosis of β-thalassemia by chip-based capillary electrophoresis;Prenatal Diagnosis;2008

4. Rapid carrier screening for β-thalassemia by single-step allele-specific PCR and detection;Clinical Biochemistry;2007-03

5. Characterisation and confirmation of rare beta-thalassaemia mutations in the Malay, Chinese and Indian ethnic groups in Malaysia;Pathology;2006-10

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