Advanced search
Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 35, 2011 - Issue 2
Submit an article Journal homepage
110
Views
4
CrossRef citations to date
0
Altmetric
Short Communication

Hb Lynwood [α107(G14) (–T) (α2) HBA2:c.323delT)] in Conjunction with the α3.7 Deletion Produces a Moderately Severe α-Thalassemia Phenotype

Jill Finlayson Department of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia; School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Perth, WA, AustraliaCorrespondence[email protected]
,
Reza Ghassemifar Department of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia; School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Perth, WA, Australia
,
Paula Holmes Department of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia
,
Dianne Grey Department of Haematology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia
,
Christopher Newbound Department of Diagnostic Molecular Genetics, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia
,
Nicole Pell Department of Diagnostic Molecular Genetics, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia
,
Michelle Jennens Department of Diagnostic Molecular Genetics, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia
,
Claire Macaulay Department of Diagnostic Molecular Genetics, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia
,
Laura Greenwood Department of Diagnostic Molecular Genetics, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia
&
John Beilby Department of Diagnostic Molecular Genetics, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Perth, WA, Australia; School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Perth, WA, Australia
 show all
Pages 142-146 | Received 13 Dec 2010, Accepted 07 Jan 2011, Published online: 21 Mar 2011

Citations (4)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (3)

Runa M. Grimholt, Bente Fjeld & Olav Klingenberg. (2021) Hemoglobinopathy gone astray—three novel forms of α-thalassemia in Norwegian patients characterized by quantitative real-time PCR and DNA sequencing. Scandinavian Journal of Clinical and Laboratory Investigation 81:8, pages 670-678.
Read now
Talal Qadah, Jill Finlayson, Emma North & Reza Ghassemifar. (2015) Molecular Characterization of Hb Hamilton Hill (HBA2: c.388delC), a Novel HBA2 Variant Generating a Premature Termination Codon and Truncated HBA2 Chain. Hemoglobin 39:2, pages 88-94.
Read now
Elisabeth Saller, Fabrizio Dutly & Hannes Frischknecht. (2015) Two Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype. Hemoglobin 39:2, pages 144-146.
Read now

Articles from other publishers (1)

Giovanna Cardiero, Gennaro Musollino, Romeo Prezioso & Giuseppina Lacerra. (2021) mRNA Analysis of Frameshift Mutations with Stop Codon in the Last Exon: The Case of Hemoglobins Campania [α1 cod95 (−C)] and Sciacca [α1 cod109 (−C)]. Biomedicines 9:10, pages 1390.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.