Advanced search
Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 21, 1997 - Issue 6
Submit an article Journal homepage
32
Views
7
CrossRef citations to date
0
Altmetric
Original Article

Mild Thalassemia Intermedia Resulting from a New Insertion/Frameshift Mutation in the β-Globin Gene

D. Williamson University, Department of Haematology, Medical Research Council Centre, Cambridge, CB2 2QH, UK; Department of Haematology, Addenbrooke's National Health Service Trust, Cambridge, CB2 2QQ, UK
,
K. P. Brown Department of Haematology, Addenbrooke's National Health Service Trust, Cambridge, CB2 2QQ, UK
,
J. V. Langdown Department of Haematology, Addenbrooke's National Health Service Trust, Cambridge, CB2 2QQ, UK
&
T. P. Baglin Department of Haematology, Addenbrooke's National Health Service Trust, Cambridge, CB2 2QQ, UK
Pages 485-493 | Received 18 Mar 1997, Accepted 14 Aug 1997, Published online: 07 Jul 2009

Citations (7)

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)

Joanne Traeger-Synodinos & Cornelis L. Harteveld. (2017) Preconception carrier screening and prenatal diagnosis in thalassemia and hemoglobinopathies: challenges and future perspectives. Expert Review of Molecular Diagnostics 17:3, pages 281-291.
Read now
Samaneh Farashi, Fariba Rad, Bahram Shahmohammadi, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2016) First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain. Hemoglobin 40:2, pages 102-107.
Read now
T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
Read now

Articles from other publishers (4)

Peng Yi, Fang Yu, Shengwei Huang, Cunli Zhong, Qiang Li, Yuan Yang, Wenqing Zhang, Chenglin Xiao & Xiangmin Xu. (2008) Identification of a novel frameshift mutation at codon 53 (−T) in the β-globin gene causing dominantly inherited β-thalassemia in a Chinese Miao family. Blood Cells, Molecules, and Diseases 41:1, pages 56-59.
Crossref
B.I. Weinstein, B. Erramouspe, D.M. Albuquerque, D.M. Oliveira, E.M. Kimura, F.F. Costa & M.F. Sonati. (2006) Hb Florida: A novel elongated C‐terminal β‐globin variant causing dominant β‐thalassemia phenotype. American Journal of Hematology 81:5, pages 358-360.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Swee Lay Thein. (1999) IS IT DOMINANTLY INHERITED β THALASSAEMIA OR JUST A β-CHAIN VARIANT THAT IS HIGHLY UNSTABLE?. British Journal of Haematology 107:1, pages 12-21.
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.