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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 2
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Short Communication

A Rapid Single-Tube Multiplex Polymerase Chain Reaction Assay for the Seven Most Prevalent α-Thalassemia Deletions and αααanti 3.7 α-Globin Gene Triplication

Arjan de Mare Medisch Spectrum Twente Hospital Group, Enschede, The Netherlands
,
Antoinette Heijs-Oude Groeneger Medisch Spectrum Twente Hospital Group, Enschede, The Netherlands
,
Sander Schuurman Medisch Spectrum Twente Hospital Group, Enschede, The Netherlands
,
Frank A.T.J.M. van den Bergh Medisch Spectrum Twente Hospital Group, Enschede, The Netherlands
&
Jennichjen Slomp Medisch Spectrum Twente Hospital Group, Enschede, The NetherlandsCorrespondence[email protected]
Pages 184-190 | Received 18 Aug 2009, Accepted 24 Dec 2009, Published online: 30 Mar 2010

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Alina Deshpande & Paul Scott White. (2012) Multiplexed nucleic acid-based assays for molecular diagnostics of human disease. Expert Review of Molecular Diagnostics 12:6, pages 645-659.
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Divashini Vijian, Wan Suriana Wan Ab Rahman, Kannan Thirumulu Ponnuraj, Zefarina Zulkafli, Rosnah Bahar, Norafiza Yasin, Syahzuwan Hassan & Ezalia Esa. (2023) Gene Mutation Spectrum among Alpha-Thalassaemia Patients in Northeast Peninsular Malaysia. Diagnostics 13:5, pages 894.
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Duantida Songdej & Suthat Fucharoen. (2022) Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment. Thalassemia Reports 12:4, pages 157-172.
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Orna Steinberg-Shemer, Jacob C. Ulirsch, Sharon Noy-Lotan, Tanya Krasnov, Dina Attias, Orly Dgany, Ruth Laor, Vijay G. Sankaran & Hannah Tamary. (2017) Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia. Molecular Case Studies 3:6, pages a001941.
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Dong-Zhi Li & Yan-Dong Yang. (2017) Invasive prenatal diagnosis of fetal thalassemia. Best Practice & Research Clinical Obstetrics & Gynaecology 39, pages 41-52.
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Andrew Turner, Jurgen Sasse & Aniko Varadi. (2015) Development and validation of a high throughput, closed tube method for the determination of haemoglobin alpha gene (HBA1 and HBA2) numbers by gene ratio assay copy enumeration-PCR (GRACE-PCR). BMC Medical Genetics 16:1.
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Mathula Thangarajh, Genyan Yang, Dana Fuchs, Maria R. Ponisio, Robert C. McKinstry, Alok Jaju, Michael J. Noetzel, James F. Casella, Emily Barron‐Casella, W. Craig Hooper, Sheree L. Boulet, Christopher J. Bean, Meredith E. Pyle, Amanda B. Payne, Jennifer Driggers, Heidi A. Trau, Bruce A. Vendt, Mark Rodeghier & Michael R. DeBaun. (2012) Magnetic resonance angiography‐defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose‐6‐phosphate dehydrogenase mutation in children with sickle cell anaemia. British Journal of Haematology 159:3, pages 352-359.
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M. Kengkate, P. Butthep, P. Kupatawintu, S. Kanunthong, W. Chantratita & O. Nathalang. (2012) Genotyping of HPA‐1 to ‐7 and ‐15 in the Thai population using multiplex PCR. Transfusion Medicine 22:4, pages 272-276.
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Heinz Troxler, Peter Kleinert, Markus Schmugge & Oliver Speer. 2012. 1 28 .
Yen-Ling Chen. (2011) Capillary electrophoresis combining three-step multiplex polymerase chain reactions for diagnosing α-thalassemia. ELECTROPHORESIS 32:3-4, pages 379-385.
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