Advanced search
Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 3-4
Submit an article Journal homepage
98
Views
7
CrossRef citations to date
0
Altmetric
Short Communications

A Second Case of Hb Fontainebleau [α21(B2)Ala→Pro] in an Individual with Microcytosis

Stephen O. Brennan Molecular Pathology Laboratory, University of Otago, Christchurch, New Zealand; Canterbury Health Laboratories, Christchurch, New ZealandCorrespondence[email protected]
,
Tim Chan Canterbury Health Laboratories, Christchurch, New Zealand
,
Sheila Ryken Diagnostic Medlab, Auckland, New Zealand
&
Anna Ruskova Diagnostic Medlab, Auckland, New Zealand
Pages 258-261 | Received 04 Feb 2009, Accepted 24 Mar 2009, Published online: 15 Sep 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)

Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
Read now
Abbas Khosravi, Mohammadali Jalali-Far, Najmaldin Saki, Hossein Hosseini, Hamid Galehdari, Omid Kiani-Ghalesardi, Mostafa Paridar, Azita Azarkeivan & Kabir Magaji-Hamid. (2016) Evaluation of α-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran. Hemoglobin 40:2, pages 113-117.
Read now
Andrew Turner, Jurgen Sasse & Aniko Varadi. (2014) Hb Fontainebleau (HBA2: c.64G > C) in the United Arab Emirates. Hemoglobin 38:3, pages 216-220.
Read now

Articles from other publishers (4)

H. Jalali, S.T. Rasouli, M. Najafi, H. Karami, M.R. Mahdavi & M. Mahdavi. (2020) A report of Hb Fontainebleau [α21 (B2) Ala > Pro] as a result of founder effect phenomenon. Gene Reports 19, pages 100587.
Crossref
Ahmet Genç, Yusuf Sevgiler, Süleyman Bayram & Eyyüp Rencüzoğulları. (2016) The prevalence and genotypes of alpha-thalassemia in Adıyaman: two rare alpha variants. Turkish Journal of Biochemistry 41:6, pages 467-472.
Crossref
Karina Rodríguez-Capote, Mathew P. Estey, Vilte Barakauskas, Pierre Bordeleau, Cathie-Lou Christensen, Peter Zuberbuhler & Trefor N. Higgins. (2015) A novel double heterozygous Hb Fontainebleau/HbD Punjab hemoglobinopathy. Clinical Biochemistry 48:13-14, pages 904-907.
Crossref
Dipti S Upadhye, Dipty Jain, Sona B Nair, Anita H Nadkarni, Kanjaksha Ghosh & Roshan B Colah. (2012) First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders. Journal of Clinical Pathology 65:7, pages 654-659.
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.